<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.0 20040830//EN" "journalpublishing.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="2.0" xml:lang="en" article-type="research-article"><front><journal-meta><journal-id journal-id-type="nlm-ta">JMIR Res Protoc</journal-id><journal-id journal-id-type="publisher-id">ResProt</journal-id><journal-id journal-id-type="index">5</journal-id><journal-title>JMIR Research Protocols</journal-title><abbrev-journal-title>JMIR Res Protoc</abbrev-journal-title><issn pub-type="epub">1929-0748</issn><publisher><publisher-name>JMIR Publications</publisher-name><publisher-loc>Toronto, Canada</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">v15i1e76783</article-id><article-id pub-id-type="doi">10.2196/76783</article-id><article-categories><subj-group subj-group-type="heading"><subject>Protocol</subject></subj-group></article-categories><title-group><article-title>Comparative Evaluation of the Antibacterial Efficacy of Metronidazole, Chlorhexidine, and Normal Saline as Laser- and Sonic-Activated Intracanal Irrigants Against <italic>Enterococcus faecalis</italic>: In Vitro Study Protocol</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name name-style="western"><surname>Deshmukh</surname><given-names>Sharvari</given-names></name><degrees>MDS</degrees><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Patel</surname><given-names>Aditya</given-names></name><degrees>MDS, PhD</degrees><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Conservative Dentistry and Endodontics, Sharad Pawar Dental College &#x0026; Hospital</institution><addr-line>DMIHER Campus, Sawangi-Meghe</addr-line><addr-line>Wardha</addr-line><country>India</country></aff><contrib-group><contrib contrib-type="editor"><name name-style="western"><surname>Sarvestan</surname><given-names>Javad</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="reviewer"><name name-style="western"><surname>Mahmoud</surname><given-names>Randa Salah Gomaa</given-names></name></contrib><contrib contrib-type="reviewer"><name name-style="western"><surname>Amusa</surname><given-names>Tope</given-names></name></contrib></contrib-group><author-notes><corresp>Correspondence to Sharvari Deshmukh, MDS, Department of Conservative Dentistry and Endodontics, Sharad Pawar Dental College &#x0026; Hospital, DMIHER Campus, Sawangi-Meghe, Wardha, India, 91 9373773020; <email>sharvarid1600@gmail.com</email></corresp></author-notes><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>7</day><month>1</month><year>2026</year></pub-date><volume>15</volume><elocation-id>e76783</elocation-id><history><date date-type="received"><day>30</day><month>04</month><year>2025</year></date><date date-type="rev-recd"><day>08</day><month>08</month><year>2025</year></date><date date-type="accepted"><day>26</day><month>08</month><year>2025</year></date></history><copyright-statement>&#x00A9; Sharvari Deshmukh, Aditya Patel. Originally published in JMIR Research Protocols (<ext-link ext-link-type="uri" xlink:href="https://www.researchprotocols.org">https://www.researchprotocols.org</ext-link>), 7.1.2026. </copyright-statement><copyright-year>2026</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on <ext-link ext-link-type="uri" xlink:href="https://www.researchprotocols.org">https://www.researchprotocols.org</ext-link>, as well as this copyright and license information must be included.</p></license><self-uri xlink:type="simple" xlink:href="https://www.researchprotocols.org/2026/1/e76783"/><abstract><sec><title>Background</title><p>The persistence of <italic>Enterococcus faecalis</italic> is a significant challenge in endodontic therapy, due to its ability to form biofilms and penetrate the dentinal tubules, frequently leading to treatment failures. Therefore, despite the proven antimicrobial activity of metronidazole (MTR) and chlorhexidine (CHX), the resilience of <italic>E. faecalis</italic> necessitates integrating activation techniques. Laser and sonic activation methods show promise in enhancing the antibacterial performance of irrigants. However, studies on the activation-enhanced efficacy of MTR, CHX, and saline remain limited.</p></sec><sec><title>Objective</title><p>This study aimed to compare the antibacterial efficacy of MTR, CHX, and normal saline as intracanal irrigants when activated by laser and sonic techniques against <italic>E. faecalis</italic> in extracted human mandibular premolars.</p></sec><sec sec-type="methods"><title>Methods</title><p>It is a laboratory-based in vitro experimental study involving extracted human teeth. Ninety freshly extracted single-rooted mandibular premolars will be obtained, decoronated, and biomechanically prepared. Canals will be inoculated with <italic>E. faecalis</italic> (ATCC 29212) and incubated for 7 days to allow biofilm formation. The teeth will then be randomly divided into 3 main groups ([MTR], [CHX], and saline), each subdivided based on the activation method used (laser or sonic). Irrigation protocols will be standardized, and pre- and postirrigation bacterial samples will be collected on paper points and cultured on brain heart infusion agar. Colony-forming units will be counted to evaluate antibacterial efficacy.</p></sec><sec sec-type="results"><title>Results</title><p>As of June 2025, ethical approval for the study has been obtained. Sample collection of extracted human teeth commenced in July 2025, and 90 extracted teeth have been collected as of January 2026, corresponding to the planned sample size. Laboratory procedures and data analysis have not yet commenced.</p></sec><sec sec-type="conclusions"><title>Conclusions</title><p>This study aims to provide evidence-based insights into optimizing root canal disinfection protocols by evaluating and comparing the synergistic effects of antimicrobial agents and advanced activation techniques. The findings could contribute significantly to improving endodontic treatment outcomes and reducing the incidence of persistent infections caused by <italic>E. faecalis</italic>.</p></sec><sec sec-type="registered-report"><title>International Registered Report Identifier (IRRID)</title><p>PRR1-10.2196/76783</p></sec></abstract><kwd-group><kwd>Enterococcus faecalis</kwd><kwd>metronidazole</kwd><kwd>chlorhexidine</kwd><kwd>sonic activation</kwd><kwd>laser activation</kwd><kwd>root canal disinfection</kwd><kwd>intracanal irrigants</kwd><kwd>endodontic treatment</kwd></kwd-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>The combined action of intracanal drugs and chemomechanical preparation reduces or eliminates bacteria during root canal therapy (RCT) [<xref ref-type="bibr" rid="ref1">1</xref>]. The mechanical action of tools and the flow and backflow of irrigating solutions are used to remove bacteria and other irritants from the root canal&#x2019;s boundaries [<xref ref-type="bibr" rid="ref2">2</xref>]. A common and successful endodontic treatment for pulpitis and apical periodontitis is conventional root canal therapy, which uses biomechanical equipment to remove affected tooth pulp and dentin tissue while using antibiotics and antibacterial materials to eradicate germs [<xref ref-type="bibr" rid="ref3">3</xref>].</p><p><italic>Enterococcus faecalis</italic> has been detected in approximately 4%-40% of primary endodontic infections, indicating its significant role in persistent and recurrent root canal infections, especially in cases of treatment-resistant apical periodontitis [<xref ref-type="bibr" rid="ref4">4</xref>,<xref ref-type="bibr" rid="ref5">5</xref>]. Despite root canal treatment, up to 90% of teeth may retain residual infection. In the twenty-first century, with rising advancements in RCT, the complete eradication of <italic>E. faecalis</italic> remains challenging due to its ability to survive under adverse conditions, with 2 main pillars of its survival being penetrating dentinal tubules and forming biofilms that resist conventional antimicrobial strategies. Its biofilms are notably resilient to commonly used intracanal agents like sodium hypochlorite and calcium hydroxide [<xref ref-type="bibr" rid="ref6">6</xref>].</p><p>Many medications, including metronidazole (MTR) and chlorhexidine (CHX), have been used to treat oral diseases because they are excellent at inhibiting bacteria and biofilms. A broad-spectrum antibiotic that targets both anaerobic bacteria and protozoa, MTR is a nitroimidazole molecule. In addition to Gram-positive and Gram-negative bacilli, it exhibits strong antibacterial activity against anaerobic cocci. Both topical and systemic applications have been made in the treatment of periodontal disease. The anatomical complexity of the RCT may, however, harbor germs and remaining pulp tissue following RCT, potentially leading to treatment failure [<xref ref-type="bibr" rid="ref7">7</xref>].</p><p>CHX is a cationic biguanide with broad-spectrum coverage. It has activity against both Gram-positive and Gram-negative bacteria. At low concentrations with a range between 0.2% and 0.06%, CHX shows bacteriostatic properties. At high concentrations, more than 0.12%, it depicts bactericidal activity, antifungal properties, and some antiviral properties. Its effect is not hampered by biological fluids such as blood, and it works for up to 48 hours after application. It acts by penetrating the bacterial cell membrane, causing cytoplasmic leakage at lower concentrations and precipitating nucleic acid at higher concentrations [<xref ref-type="bibr" rid="ref8">8</xref>].</p><p>Normal saline, although lacking intrinsic antimicrobial properties, is included in this study as a negative control to isolate and evaluate the specific contribution of activation techniques (laser and sonic) independent of chemical disinfection. Its inclusion enables assessment of whether activation alone can produce any measurable reduction in bacterial load.</p><p>The distribution method, in conjunction with the irrigant&#x2019;s characteristics, affects the irrigation efficacy [<xref ref-type="bibr" rid="ref9">9</xref>]. Irrigant activation in endodontic procedures pertains to the use of various energy forms&#x2014;mechanical, sonic, ultrasonic, or other physical modalities&#x2014;to enhance the dynamic movement and distribution of irrigating solutions throughout the intricately structured root canal system. Evidence from systematic reviews and meta-analyses indicates that the use of activation, regardless of the specific device or mechanism employed, significantly improves the efficacy of debris and smear layer removal. Consequently, activation is recognized as an integral phase in the chemo-mechanical debridement process, contributing to the overall success of root canal disinfection [<xref ref-type="bibr" rid="ref10">10</xref>]. In contrast to ultrasonic irrigation, sonic irrigation uses a lower frequency (1&#x2010;10 kHz). As a result, shear wall stresses and fluid velocity are reduced. Conversely, sonic activation produces noticeably more amplitude (horizontal tip displacement) [<xref ref-type="bibr" rid="ref11">11</xref>].</p><p>In recent years, nonsurgical RCT has made greater use of laser technology. When used in conjunction with chemical solutions, its high power and distinct coherent rays are helpful during the root canal cleaning and disinfection phase. It has been demonstrated that a laser can effectively activate a root canal irrigant by causing mechanical disruptions [<xref ref-type="bibr" rid="ref12">12</xref>]. The 940 nm diode laser is frequently used in dentistry clinics due to its compact size, portability, affordability, and broad variety of oral medicine applications. Bacterial cell walls can be destroyed by the bactericidal photothermal disrupting impact of its radiation [<xref ref-type="bibr" rid="ref13">13</xref>]. Since water and hydroxyapatite are the primary components of dentin, the 940 nm wavelength has low absorption coefficients in water (about &#x03BC;a=0.04&#x2010;0.05 cm<sup>&#x2212;1</sup>), which allows the laser beam to penetrate deeply into dentin (over 1000 &#x03BC;m) and kill distant bacteria [<xref ref-type="bibr" rid="ref13">13</xref>,<xref ref-type="bibr" rid="ref14">14</xref>].</p><p>It has been observed in previous studies that the use of CHX and MTR as intracanal irrigants showed optimal results. However, studies with MTR as an intracanal irrigant with different activation methods need to be explored. Although metronidazole has demonstrated antimicrobial efficacy as an intracanal irrigant, prior studies have primarily evaluated it in static or nonactivated forms. So, there is a need for research that compares the antibacterial effectiveness of MTR, CHX, and normal saline as intracanal irrigants, which are activated by laser and sonic activation methods, against <italic>E. faecalis</italic>. This comparison will help determine the most effective activation technique for enhancing the antibacterial effectiveness of these irrigants, ultimately contributing to more reliable and durable endodontic treatments, improving treatment success rates, and reducing the incidence of persistent infections associated with this resilient bacterium. This study might address this critical gap by evaluating the synergistic effects of activation-enhanced MTR, thereby expanding current understanding and potentially informing more effective endodontic disinfection protocols.</p><p>This in vitro study aims to compare the antibacterial efficacy of MTR, CHX, and normal saline as intracanal irrigants when activated using laser and sonic techniques against <italic>E. faecalis</italic> in extracted human mandibular premolars. The study evaluates the effectiveness of each irrigant with both laser and sonic activation techniques to determine their potential in eliminating bacterial contamination from the root canal system. It is hypothesized that laser and sonic activation will significantly enhance the antibacterial efficacy of these irrigants, with notable differences among the groups.</p><p>The null hypothesis for the study assumes that, &#x201C;there will be no significant effect of laser and sonic activation on the antibacterial efficacy of MTR, CHX, and saline as intracanal irrigants in eradicating Enterococcus faecalis in root canal treatments&#x201D; while the alternative hypothesis suggests, &#x201C;laser and sonic activation will significantly enhance the antibacterial efficacy of MTR, CHX, and saline as intracanal irrigants in eradicating Enterococcus faecalis in root canal treatments.&#x201D;</p></sec><sec id="s2" sec-type="methods"><title>Methods</title><sec id="s2-1"><title>Study Design</title><p>This study used a comparative in vitro study design.</p></sec><sec id="s2-2"><title>Materials</title><p>The materials to be used in the current study are listed in <xref ref-type="other" rid="box1">Textbox 1</xref>.</p><boxed-text id="box1"><title> Materials to be used for microbial inoculation, irrigation, activation, and root canal preparation.</title><list list-type="bullet"><list-item><p>Microbiological sample preparation:</p></list-item></list><list list-type="simple"><list-item><p><named-content content-type="indent">&#x2003;</named-content>1. Strains of <italic>Enterococcus faecalis</italic></p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>2. Brain heart infusion (BHI) agar media</p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>3. Incubator</p></list-item></list><list list-type="bullet"><list-item><p>Irrigants:</p></list-item></list><list list-type="simple"><list-item><p><named-content content-type="indent">&#x2003;</named-content>1. Chlorhexidine (CHX)</p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>2. Metronidazole (MTR)</p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>3. Normal saline</p></list-item></list><list list-type="bullet"><list-item><p>Activation devices:</p></list-item></list><list list-type="simple"><list-item><p><named-content content-type="indent">&#x2003;</named-content>1. Sonic activation device</p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>2. Diode laser</p></list-item></list><list list-type="bullet"><list-item><p>For sample preparation:</p></list-item></list><list list-type="simple"><list-item><p><named-content content-type="indent">&#x2003;</named-content>1. Protaper Universal treatment rotary files (for biomechanical preparation)</p></list-item><list-item><p><named-content content-type="indent">&#x2003;</named-content>2. Paper points</p></list-item></list><p/></boxed-text></sec><sec id="s2-3"><title>Sample Size</title><p>The sample size was estimated based on previously published data [<xref ref-type="bibr" rid="ref15">15</xref>], assuming a power of 80%, significance level of 5%, and a mean difference of 23 in colony-forming unit (CFU) between groups. Group SDs were 17.33 and 2.81. These assumptions resulted in a minimum of 15 samples per subgroup. The complete sample size formula, derivation, and calculation steps are provided in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>. Although the reference study involved a different irrigant (BioPure MTAD) and microbial model, it was the most comparable source available and served as a reasonable baseline for estimating variability in CFU reduction in the current study.</p></sec><sec id="s2-4"><title>Sample Selection</title><p>The inclusion and exclusion criteria are given in <xref ref-type="other" rid="box2">Textbox 2</xref>.</p><boxed-text id="box2"><title> Inclusion and exclusion criteria.</title><p>Inclusion Criteria</p><list list-type="bullet"><list-item><p>Freshly extracted single-rooted permanent mandibular lower premolar teeth with closed apex, free from caries, fracture, and previous endodontic treatment.</p></list-item></list><p>Exclusion Criteria</p><list list-type="bullet"><list-item><p>Teeth with visible cracks, abnormal morphology.</p></list-item><list-item><p>Teeth with developmental anomalies.</p></list-item><list-item><p>Teeth with external and internal resorption.</p></list-item><list-item><p>Teeth with multiple roots.</p></list-item><list-item><p>Teeth with calcified canals.</p></list-item></list></boxed-text></sec><sec id="s2-5"><title>Sample Allocation</title><p>Distribution of sample size was 90. The specimens will be randomly divided into 3 groups and 6 subgroups (<xref ref-type="table" rid="table1">Table 1</xref>).</p><table-wrap id="t1" position="float"><label>Table 1.</label><caption><p>Sample distribution across experimental groups based on irrigant type and activation methodology.</p></caption><table id="table1" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Groups and subgroups</td><td align="left" valign="bottom">Samples (n)</td></tr></thead><tbody><tr><td align="left" valign="top">Group I: 5 ml of 0.5% MTR<sup><xref ref-type="table-fn" rid="table1fn1">a</xref></sup> as an irrigant for 3 min</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IA: Laser activation for 30 sec</td><td align="left" valign="top">15</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IB: Sonic activation</td><td align="char" char="." valign="top">15</td></tr><tr><td align="left" valign="top">Group II: 5 ml of 2% CHX<sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup> as an irrigant for 3 min</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IIA: Laser activation</td><td align="left" valign="top">15</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IIB: Sonic activation</td><td align="char" char="." valign="top">15</td></tr><tr><td align="left" valign="top">Group III: 5 ml of normal saline as an irrigant for 3 min</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IIIA: Laser activation</td><td align="left" valign="top">15</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Subgroup IIIB: Sonic activation</td><td align="char" char="." valign="top">15</td></tr></tbody></table><table-wrap-foot><fn id="table1fn1"><p><sup>a</sup>MTR: metronidazole.</p></fn><fn id="table1fn2"><p><sup>b</sup>CHX: chlorhexidine.</p></fn></table-wrap-foot></table-wrap></sec><sec id="s2-6"><title>Groups</title><p>This study aims to evaluate the antibacterial efficacy of 3 irrigant solutions&#x2014;MTR, CHX, and normal saline&#x2014;against <italic>E. faecalis</italic> using 2 activation methods (laser and sonic). The study will involve a total sample size of 90, divided into 3 main groups based on the intracanal irrigants used, and will be further divided into subgroups based on the activation protocol employed.</p></sec><sec id="s2-7"><title>Sample Preparation</title><p>90 extracted single-rooted premolar teeth will be obtained from healthy patients with informed consent. Extractions will be performed for reasons unrelated to dental pathology, such as orthodontic treatment, prosthetic rehabilitation (eg, to facilitate fixed or removable partial dentures), esthetic concerns, or to preserve adjacent vital structures. Teeth exhibiting caries, restorations, root resorption, calcifications, or a history of endodontic treatment will be excluded from the study. In case of sample loss due to contamination, fracture, or invalid measurements during any phase of the study, replacements will be made from the remaining pool of eligible specimens to maintain balanced group sizes. All such instances will be recorded and reported.</p></sec><sec id="s2-8"><title>Tooth Decoronation and Canal Preparation</title><p>The teeth will then be cleaned and sterilized, removing any residual tissue. Following the removal of any remaining tissue, the teeth will be washed and sterilized before being kept at room temperature in a 0.1% thymol solution until the experimental phase. To achieve a uniform root length of 13 mm, the crowns will thereafter be decoronated using a diamond disc. To get the working length, 1 mm will be subtracted from the total root length. From the total root length to establish the working length, 1 mm will be deducted. Root canal shaping will be carried out up to the F2 instrument.</p></sec><sec id="s2-9"><title>Inoculation of <italic>E. faecalis</italic></title><p>The strain of <italic>E. faecalis</italic> (ATCC 29212) used in this study will be obtained from the Department of Microbiology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences (Deemed to be University), Wardha, India. The strains will be cultured and inoculated into the prepared canals of all samples. The samples will be incubated for 7 days to allow biofilm formation. Before irrigation, sterile paper points will be inserted into each canal for 60 seconds to collect pretreatment samples. These paper points will then be transferred to BHI Agar media and incubated for 48 hours. The colonies will then be counted using the classic bacterial counting method. Preirrigation samples will be taken. The inoculated teeth will then be randomly assigned to their respective groups and subgroups.</p></sec><sec id="s2-10"><title>Biosafety Measures</title><p>All procedures involving <italic>E. faecalis</italic> will be conducted in a biosafety level-2 laboratory, following institutional biosafety guidelines. Sterile gloves, masks, and lab coats will be worn during microbial handling. All contaminated instruments and waste will be autoclaved and discarded in biohazard disposal systems. Teeth will be stored in 0.1% thymol prior to use to maintain sterility.</p></sec><sec id="s2-11"><title>Irrigation Protocol</title><p>Irrigation will involve 3% sodium hypochlorite (Shivam, India), followed by 3 ml of 17% ethylene diamine tetra acetic acid for 1 minute to remove the smear layer, and subsequent irrigation protocol of every group will then be followed by using 5 ml of respective irrigants of 0.5% MTR, 2% CHX, and saline for 3 minutes accompanied by laser sonic activation with the EndoActivator (Dentsply Maillefer, Switzerland) operating at 10,000 cycles per minute (167 Hz) using a medium-sized tip (25/04). Each canal will be agitated for 30 seconds continuously. Laser activation will be performed using a diode laser (Biolase Epic X, Biolase Inc., USA) operating at a wavelength of 980 nm and a power setting of 1.5 W in pulsed mode. A 200-&#x00B5;m flexible fiber tip will be introduced 1 mm short of the working length. Each canal will undergo 3 cycles of laser activation, with each cycle lasting 5 seconds, followed by a 10-second interval between cycles. Postirrigation samples will be collected with the help of paper points and deposited into BHI Agar media and incubated for 48 hours.</p></sec><sec id="s2-12"><title>Outcome Measures</title><p>The colonies will then be counted using the classic bacterial counting method to evaluate bacterial reduction. The data collected will then be subjected to statistical analysis. Scanning electron microscopy can offer visual confirmation of biofilm formation. The present study will follow a validated 7-day <italic>E. faecalis</italic> incubation protocol, as established in previous literature. In phase I of the study, antimicrobial efficacy will be quantitatively assessed using CFU counts, which provide a reliable and clinically relevant measure.</p><p>The procedure to be followed is depicted in the following flowchart (<xref ref-type="fig" rid="figure1">Figure 1</xref>).</p><fig position="float" id="figure1"><label>Figure 1.</label><caption><p>Experimental protocol workflow. CFU: colony-forming units; <italic>E. faecalis</italic>: <italic>Enterococcus faecalis</italic>.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="resprot_v15i1e76783_fig01.png"/></fig></sec><sec id="s2-13"><title>Statistical Analysis</title><p>The dataset will undergo both summarization and advanced statistical interpretation. Normality of data distribution will be assessed using the Shapiro-Wilk test. Analytical tools will include the &#x1D712;<sup>2</sup> method, Student&#x2019;s <italic>t</italic> tests (applicable for both related and independent samples), as well as one-way ANOVA followed by Tukey&#x2019;s postanalysis comparisons. All statistical procedures and visual data representations will be executed using SPSS (version 27.0) and GraphPad Prism (version 7.0). A probability value <italic>P</italic>&#x003C;.05 will be treated as indicative of a statistically meaningful result. The statistical methods to be applied are illustrated in <xref ref-type="fig" rid="figure2">Figure 2</xref>.</p><fig position="float" id="figure2"><label>Figure 2.</label><caption><p>Stepwise statistical analysis workflow. CFU: colony-forming units; CHX: chlorhexidine; NS: normal saline.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="resprot_v15i1e76783_fig02.png"/></fig></sec><sec id="s2-14"><title>Ethical Considerations</title><p>Ethical approval for the study was obtained from the Institutional Ethical Committee of Datta Meghe Institute of Higher Education &#x0026; Research, Sawangi, Wardha (Approval number: DMIHER(DU)/IEC/2025/545 dated: 07/02/2025). Written informed consent will be obtained from patients prior to extraction regarding the use of extracted teeth for research purposes in this study. All extracted teeth will be deidentified before inclusion in the experimental protocol to maintain complete anonymity of the donors. No financial or nonfinancial compensation was provided to the patients for participation in this study or for the use of extracted teeth for research purposes.</p></sec></sec><sec id="s3" sec-type="results"><title>Results</title><sec id="s3-1"><title>Overview</title><p>Ethical approval was obtained in June 2025. Sample collection of extracted human teeth commenced in July 2025, and 90 extracted teeth have been collected as of January 2026, corresponding to the planned sample size. Laboratory procedures and data analysis have not yet commenced.</p></sec><sec id="s3-2"><title>Primary Outcome Measure</title><p>The primary outcome measure was the evaluation and comparison of reduction in the CFU count of <italic>E. faecalis</italic> following irrigation by MTR with sonic and laser activation techniques with that of CHX and normal saline.</p></sec><sec id="s3-3"><title>Secondary Outcome Measure</title><p>The secondary outcome measure was to determine the most effective combination of irrigant and activation technique to target and eliminate <italic>E. faecalis</italic> residing in the root canal space effectively.</p></sec></sec><sec id="s4" sec-type="discussion"><title>Discussion</title><p>Achieving successful root canal outcomes requires the meticulous elimination of all microorganisms harbored within the complicated architecture of the root canal system. Despite advancements in irrigation protocols and antimicrobial strategies, <italic>E. faecalis</italic> remains a major causative agent in treatment failures due to its exceptional resistance and adaptability [<xref ref-type="bibr" rid="ref1">1</xref>,<xref ref-type="bibr" rid="ref2">2</xref>]. This facultative anaerobe is known for its ability to penetrate dentinal tubules, survive in nutrient-deprived environments, and resist common intracanal medicaments, including calcium hydroxide [<xref ref-type="bibr" rid="ref3">3</xref>]. These characteristics underscore the need for not only potent antibacterial agents but also effective activation techniques to enhance their intracanal performance.</p><p>In this context, MTR and CHX have emerged as promising irrigants. MTR, a nitroimidazole derivative, is especially effective against anaerobic bacteria and has been used in both systemic and local applications in dental practice [<xref ref-type="bibr" rid="ref4">4</xref>]. Although its antibacterial spectrum includes <italic>E. faecalis</italic>, the clinical efficacy of MTR may be compromised when used without adjunct activation techniques due to its limited ability to penetrate biofilms [<xref ref-type="bibr" rid="ref5">5</xref>]. CHX, on the other hand, is a broad-spectrum cationic biguanide that retains its activity in the presence of organic matter and has substantivity, remaining active for prolonged durations postapplication [<xref ref-type="bibr" rid="ref6">6</xref>]. It has shown superior performance in reducing microbial load within the canal system, especially when used at concentrations above 0.12% [<xref ref-type="bibr" rid="ref6">6</xref>].</p><p>However, the delivery and penetration of these irrigants into canal irregularities are critically dependent on activation techniques. Sonic and laser activation have been shown to improve irrigant flow dynamics, resulting in deeper penetration and enhanced disinfection. Sonic activation systems such as the EndoActivator operate at lower frequencies (1&#x2010;10 kHz), creating hydrodynamic agitation that improves smear layer and debris removal. Their greater amplitude allows more effective lateral displacement of irrigants within the root canal [<xref ref-type="bibr" rid="ref9">9</xref>].</p><p>Laser activation, particularly using diode lasers at 940 nm, represents a significant advancement in endodontic disinfection. The unique properties of laser energy&#x2014;specifically its ability to induce photothermal and photoacoustic effects&#x2014;result in deeper penetration into dentin and effective bacterial cell wall disruption [<xref ref-type="bibr" rid="ref10">10</xref>,<xref ref-type="bibr" rid="ref11">11</xref>]. Unlike conventional irrigants whose efficacy is often limited to the main canal, laser activation facilitates disinfection in otherwise inaccessible microanatomical structures, including lateral canals and apical ramifications [<xref ref-type="bibr" rid="ref12">12</xref>]. Furthermore, diode lasers are advantageous due to their compact size, cost-effectiveness, and compatibility with clinical settings [<xref ref-type="bibr" rid="ref11">11</xref>].</p><p>The present investigation is designed to explore an under-researched area by directly assessing the antimicrobial performance of MTR, CHX, and saline when activated via laser and sonic methods. While previous studies have highlighted the individual efficacy of these irrigants and activation methods, few have explored their synergistic impact, particularly with MTR as the primary irrigant. Given that metronidazole&#x2019;s efficacy is enhanced in anaerobic conditions and that <italic>E. faecalis</italic> can adapt to both aerobic and anaerobic environments, activation becomes a pivotal factor in optimizing its bactericidal action [<xref ref-type="bibr" rid="ref4">4</xref>,<xref ref-type="bibr" rid="ref5">5</xref>].</p><p>Moreover, CHX&#x2019;s substantivity and ability to disrupt microbial membranes at higher concentrations may complement the mechanical benefits of sonic and laser activation, potentially yielding superior outcomes compared to passive irrigation techniques [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref8">8</xref>]. In contrast, saline serves as a control, allowing for a clear demarcation of the role of activation in enhancing antibacterial performance.</p><p>Previous studies support the antibacterial potential of MTR as an endodontic irrigant. Amin et al [<xref ref-type="bibr" rid="ref16">16</xref>] reported significant bacterial reduction with 5 ml of 0.5% MTR and 2% CHX in primary teeth, with saline showing no effect. Dubey et al [<xref ref-type="bibr" rid="ref17">17</xref>] found MTR effective against <italic>Bacteroides fragilis</italic> and <italic>Propionibacterium acnes</italic>, while BioPure MTAD showed greater efficacy against <italic>E. faecalis</italic> and <italic>Candida albicans</italic>, highlighting MTR&#x2019;s limited spectrum. Shweta et al [<xref ref-type="bibr" rid="ref15">15</xref>] demonstrated that the combination of 0.5% MTR and 2% glutaraldehyde exhibited enhanced antibacterial action over saline, with ultrasonic activation outperforming hand irrigation. These findings justify evaluating the combination of activated MTR and CHX in the present study to enhance efficacy against <italic>E. faecalis</italic>.</p><p>The incubation protocol is based on previously validated studies, such as those by Amin et al [<xref ref-type="bibr" rid="ref16">16</xref>] and Shweta et al [<xref ref-type="bibr" rid="ref15">15</xref>], which demonstrated reliable biofilm formation of <italic>E. faecalis</italic> following a 7-day incubation period under controlled conditions. These studies used similar in vitro infection models without requiring SEM confirmation to validate biofilm maturity, relying instead on established microbiological protocols and CFU quantification. As this study constitutes Phase I of a multiphase research design, our primary aim is to evaluate the antibacterial efficacy of different irrigants activated by laser and sonic techniques. While SEM is not incorporated in this phase due to resource constraints and focus on microbial reduction outcomes, Phase II is planned to include SEM analysis of selected samples to confirm dentinal tubule penetration and biofilm ultrastructure, thereby augmenting the qualitative depth of findings.</p><p>The exploration of enhanced antimicrobial strategies in endodontics, including the use of nanoparticle-modified sealers [<xref ref-type="bibr" rid="ref18">18</xref>], reflects a broader effort to improve root canal disinfection outcomes. While the present study evaluates the in vitro efficacy of various irrigant&#x2013;activation combinations, it also underscores the importance of translating such findings into clinical education and practice. As highlighted by Haupt and Kanzow [<xref ref-type="bibr" rid="ref19">19</xref>], a persistent gap often exists between theoretical understanding and practical competence in endodontics, particularly during preclinical training. Addressing this gap may be critical for the successful clinical application of evidence-based disinfection protocols.</p><p>Overall, the findings of this study are anticipated to contribute significantly to clinical endodontics by providing evidence for more effective disinfection protocols. If MTR, when activated, proves comparable or superior to CHX, it may represent a cost-effective and biocompatible alternative for routine endodontic practice. This integrated approach may offer a promising direction toward reducing persistent infections and improving long-term treatment outcomes.</p></sec></body><back><ack><p>The author expresses sincere gratitude to the esteemed guide for constant support, expert guidance, and encouragement throughout the course of this research. The author is thankful to the Department of Conservative Dentistry and Endodontics, Sharad Pawar Dental College &#x0026; Hospital, Datta Meghe Institute of Higher Education &#x0026; Research, Sawangi, Wardha, for providing the necessary facilities and resources to carry out this study. The author is also grateful to the faculty members and laboratory technicians for their valuable suggestions and moral support. Special thanks are extended to the author&#x2019;s family for their unwavering love, patience, and motivation. All authors declared that they had insufficient funding to support open access publication of this manuscript, including from affiliated organizations or institutions, funding agencies, or other organizations. JMIR Publications provided article processing fee (APF) support for the publication of this article.</p></ack><fn-group><fn fn-type="conflict"><p>None declared.</p></fn></fn-group><glossary><title>Abbreviations</title><def-list><def-item><term id="abb1">BHI</term><def><p>brain heart infusion</p></def></def-item><def-item><term id="abb2">CFU</term><def><p>colony-forming units</p></def></def-item><def-item><term id="abb3">CHX</term><def><p>chlorhexidine</p></def></def-item><def-item><term id="abb4"><italic>E. faecalis</italic></term><def><p><italic>Enterococcus faecalis</italic></p></def></def-item><def-item><term id="abb5">MTR</term><def><p>metronidazole</p></def></def-item><def-item><term id="abb6">RCT</term><def><p>root canal therapy</p></def></def-item></def-list></glossary><ref-list><title>References</title><ref id="ref1"><label>1</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Karg&#x00FC;l</surname><given-names>B</given-names> </name><name name-style="western"><surname>Tanboga</surname><given-names>I</given-names> </name><name name-style="western"><surname>Altinok</surname><given-names>B</given-names> </name></person-group><article-title>Conventional endodontic treatment of primary molars using metronidazole as an intra-canal medicament: a pilot study</article-title><source>Eur Arch Paediatr Dent</source><year>2010</year><month>08</month><volume>11</volume><issue>4</issue><fpage>196</fpage><lpage>200</lpage><pub-id pub-id-type="doi">10.1007/BF03262744</pub-id><pub-id pub-id-type="medline">20840831</pub-id></nlm-citation></ref><ref id="ref2"><label>2</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>&#x00D6;zsezer Demiry&#x00FC;rek,</surname><given-names>E</given-names> </name></person-group><article-title>Evaluation of microbial contamination of resilon and gutta-percha cones and their antimicrobial activities</article-title><source>Afr J Microbiol Res</source><year>2012</year><volume>6</volume><issue>33</issue><fpage>6275</fpage><lpage>6280</lpage><comment><ext-link ext-link-type="uri" xlink:href="http://www.academicjournals.org/AJMR/contents/2012cont/30August.htm">http://www.academicjournals.org/AJMR/contents/2012cont/30August.htm</ext-link></comment><pub-id pub-id-type="doi">10.5897/AJMR12.878</pub-id></nlm-citation></ref><ref id="ref3"><label>3</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Lee</surname><given-names>DK</given-names> </name><name name-style="western"><surname>Kim</surname><given-names>SV</given-names> </name><name name-style="western"><surname>Limansubroto</surname><given-names>AN</given-names> </name><etal/></person-group><article-title>Nanodiamond-Gutta Percha composite biomaterials for root canal therapy</article-title><source>ACS Nano</source><year>2015</year><month>11</month><day>24</day><volume>9</volume><issue>11</issue><fpage>11490</fpage><lpage>11501</lpage><pub-id pub-id-type="doi">10.1021/acsnano.5b05718</pub-id><pub-id pub-id-type="medline">26452304</pub-id></nlm-citation></ref><ref id="ref4"><label>4</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>R&#x00F4;&#x00E7;as</surname><given-names>IN</given-names> </name><name name-style="western"><surname>Siqueira</surname><given-names>JF</given-names>  <suffix>Jr</suffix></name><name name-style="western"><surname>Santos</surname><given-names>KRN</given-names> </name></person-group><article-title>Association of Enterococcus faecalis with different forms of periradicular diseases</article-title><source>J Endod</source><year>2004</year><month>05</month><volume>30</volume><issue>5</issue><fpage>315</fpage><lpage>320</lpage><pub-id pub-id-type="doi">10.1097/00004770-200405000-00004</pub-id><pub-id pub-id-type="medline">15107642</pub-id></nlm-citation></ref><ref id="ref5"><label>5</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Stuart</surname><given-names>CH</given-names> </name><name name-style="western"><surname>Schwartz</surname><given-names>SA</given-names> </name><name name-style="western"><surname>Beeson</surname><given-names>TJ</given-names> </name><name name-style="western"><surname>Owatz</surname><given-names>CB</given-names> </name></person-group><article-title>Enterococcus faecalis: its role in root canal treatment failure and current concepts in retreatment</article-title><source>J Endod</source><year>2006</year><month>02</month><volume>32</volume><issue>2</issue><fpage>93</fpage><lpage>98</lpage><pub-id pub-id-type="doi">10.1016/j.joen.2005.10.049</pub-id><pub-id pub-id-type="medline">16427453</pub-id></nlm-citation></ref><ref id="ref6"><label>6</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Evans</surname><given-names>M</given-names> </name><name name-style="western"><surname>Davies</surname><given-names>JK</given-names> </name><name name-style="western"><surname>Sundqvist</surname><given-names>G</given-names> </name><name name-style="western"><surname>Figdor</surname><given-names>D</given-names> </name></person-group><article-title>Mechanisms involved in the resistance of Enterococcus faecalis to calcium hydroxide</article-title><source>Int Endod J</source><year>2002</year><month>03</month><volume>35</volume><issue>3</issue><fpage>221</fpage><lpage>228</lpage><pub-id pub-id-type="doi">10.1046/j.1365-2591.2002.00504.x</pub-id><pub-id pub-id-type="medline">11985673</pub-id></nlm-citation></ref><ref id="ref7"><label>7</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Abou-Rass</surname><given-names>M</given-names> </name><name name-style="western"><surname>Bogen</surname><given-names>G</given-names> </name></person-group><article-title>Microorganisms in closed periapical lesions</article-title><source>Int Endod J</source><year>1998</year><month>01</month><volume>31</volume><issue>1</issue><fpage>39</fpage><lpage>47</lpage><pub-id pub-id-type="medline">9823127</pub-id></nlm-citation></ref><ref id="ref8"><label>8</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Ghosh</surname><given-names>D</given-names> </name><name name-style="western"><surname>Bhardwaj</surname><given-names>S</given-names> </name><name name-style="western"><surname>Koyalada</surname><given-names>S</given-names> </name><etal/></person-group><article-title>Comparison of efficacy of ozonated water, normal saline, and povidone-iodine after surgical removal of impacted mandibular third molars: a cross-sectional study</article-title><source>J Family Med Prim Care</source><year>2020</year><month>08</month><volume>9</volume><issue>8</issue><fpage>4139</fpage><lpage>4144</lpage><pub-id pub-id-type="doi">10.4103/jfmpc.jfmpc_534_20</pub-id><pub-id pub-id-type="medline">33110822</pub-id></nlm-citation></ref><ref id="ref9"><label>9</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Susila</surname><given-names>A</given-names> </name><name name-style="western"><surname>Minu</surname><given-names>J</given-names> </name></person-group><article-title>Activated irrigation vs. conventional non-activated irrigation in endodontics - a systematic review</article-title><source>Eur Endod J</source><year>2019</year><volume>4</volume><issue>3</issue><fpage>96</fpage><lpage>110</lpage><pub-id pub-id-type="doi">10.14744/eej.2019.80774</pub-id><pub-id pub-id-type="medline">32161895</pub-id></nlm-citation></ref><ref id="ref10"><label>10</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Virdee</surname><given-names>SS</given-names> </name><name name-style="western"><surname>Seymour</surname><given-names>DW</given-names> </name><name name-style="western"><surname>Farnell</surname><given-names>D</given-names> </name><name name-style="western"><surname>Bhamra</surname><given-names>G</given-names> </name><name name-style="western"><surname>Bhakta</surname><given-names>S</given-names> </name></person-group><article-title>Efficacy of irrigant activation techniques in removing intracanal smear layer and debris from mature permanent teeth: a systematic review and meta-analysis</article-title><source>Int Endod J</source><year>2018</year><month>06</month><volume>51</volume><issue>6</issue><fpage>605</fpage><lpage>621</lpage><pub-id pub-id-type="doi">10.1111/iej.12877</pub-id><pub-id pub-id-type="medline">29178166</pub-id></nlm-citation></ref><ref id="ref11"><label>11</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Karade</surname><given-names>P</given-names> </name><name name-style="western"><surname>Chopade</surname><given-names>R</given-names> </name><name name-style="western"><surname>Patil</surname><given-names>S</given-names> </name><etal/></person-group><article-title>Efficiency of different endodontic irrigation and activation systems in removal of the smear layer: a scanning electron microscopy study</article-title><source>Iran Endod J</source><year>2017</year><volume>12</volume><issue>4</issue><fpage>414</fpage><lpage>418</lpage><pub-id pub-id-type="doi">10.22037/iej.v12i4.9571</pub-id><pub-id pub-id-type="medline">29225634</pub-id></nlm-citation></ref><ref id="ref12"><label>12</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Juri&#x010D;</surname><given-names>IB</given-names> </name><name name-style="western"><surname>Ani&#x0107;</surname><given-names>I</given-names> </name></person-group><article-title>The use of lasers in disinfection and cleaning of root canals: a review</article-title><source>Acta Stomatol Croat</source><year>2014</year><month>03</month><volume>48</volume><issue>1</issue><fpage>6</fpage><lpage>15</lpage><pub-id pub-id-type="doi">10.15644/asc48/1/1</pub-id><pub-id pub-id-type="medline">27688346</pub-id></nlm-citation></ref><ref id="ref13"><label>13</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Tilakchand</surname><given-names>M</given-names> </name><name name-style="western"><surname>Singh</surname><given-names>NN</given-names> </name><name name-style="western"><surname>Yeli</surname><given-names>MM</given-names> </name><name name-style="western"><surname>Naik</surname><given-names>BD</given-names> </name></person-group><article-title>&#x201C;Evaluation of the antibacterial efficacy of EZLASE diode LASER on the infected root canal system:&#x201D; An in vivo study</article-title><source>J Conserv Dent</source><year>2018</year><volume>21</volume><issue>3</issue><fpage>306</fpage><lpage>310</lpage><pub-id pub-id-type="doi">10.4103/JCD.JCD_14_18</pub-id><pub-id pub-id-type="medline">29899635</pub-id></nlm-citation></ref><ref id="ref14"><label>14</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Martins</surname><given-names>MR</given-names> </name><name name-style="western"><surname>Franzen</surname><given-names>R</given-names> </name><name name-style="western"><surname>Depraet</surname><given-names>F</given-names> </name><name name-style="western"><surname>Gutknecht</surname><given-names>N</given-names> </name></person-group><article-title>Rationale for using a double-wavelength (940 nm&#x2009;+&#x2009;2780 nm) laser in endodontics: literature overview and proof-of-concept</article-title><source>Laser Dent Sci</source><year>2018</year><month>03</month><volume>2</volume><issue>1</issue><fpage>29</fpage><lpage>41</lpage><pub-id pub-id-type="doi">10.1007/s41547-017-0017-9</pub-id></nlm-citation></ref><ref id="ref15"><label>15</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Jain</surname><given-names>S</given-names> </name><name name-style="western"><surname>Thakur</surname><given-names>S</given-names> </name></person-group><article-title>Antibacterial efficacy of metronidazole and glutaraldehyde with hand and ultrasonic activation-an in vivo study</article-title><source>Unique Journal Of Medical and Dental Sciences</source><year>2013</year><access-date>2026-01-05</access-date><volume>01</volume><issue>1</issue><fpage>35</fpage><lpage>59</lpage><comment><ext-link ext-link-type="uri" xlink:href="https://ujconline.net/wp-content/uploads/2013/10/6-UJMDS-1310-Rs.pdf">https://ujconline.net/wp-content/uploads/2013/10/6-UJMDS-1310-Rs.pdf</ext-link></comment></nlm-citation></ref><ref id="ref16"><label>16</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Barakat</surname><given-names>I</given-names> </name><name name-style="western"><surname>ElPatal</surname><given-names>MA</given-names> </name><name name-style="western"><surname>Abushanan</surname><given-names>A</given-names> </name><name name-style="western"><surname>Abd Elrady</surname><given-names>BEA</given-names> </name></person-group><article-title>Antibacterial effect of metronidazole vs chlorhexidine solutions in treatment of root canals of primary anterior teeth</article-title><source>J Contemp Dent Pract</source><year>2020</year><month>04</month><day>1</day><volume>21</volume><issue>4</issue><fpage>396</fpage><lpage>399</lpage><pub-id pub-id-type="doi">10.5005/jp-journals-10024-2719</pub-id><pub-id pub-id-type="medline">32584275</pub-id></nlm-citation></ref><ref id="ref17"><label>17</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Dubey</surname><given-names>S</given-names> </name><name name-style="western"><surname>Saha</surname><given-names>SG</given-names> </name><name name-style="western"><surname>Rajkumar</surname><given-names>B</given-names> </name><name name-style="western"><surname>Dhole</surname><given-names>TK</given-names> </name></person-group><article-title>Comparative antimicrobial efficacy of selected root canal irrigants on commonly isolated microorganisms in endodontic infection</article-title><source>Eur J Dent</source><year>2017</year><volume>11</volume><issue>1</issue><fpage>12</fpage><lpage>16</lpage><pub-id pub-id-type="doi">10.4103/ejd.ejd_141_16</pub-id><pub-id pub-id-type="medline">28435359</pub-id></nlm-citation></ref><ref id="ref18"><label>18</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Mohamed</surname><given-names>A</given-names> </name><name name-style="western"><surname>Ismail</surname><given-names>E</given-names> </name><name name-style="western"><surname>Adam</surname><given-names>RZ</given-names> </name></person-group><article-title>A comparison of conventional root canal sealers with ones that use green synthesized nanoparticles for antimicrobial activity: protocol for a systematic review</article-title><source>JMIR Res Protoc</source><year>2024</year><month>10</month><day>11</day><volume>13</volume><fpage>e51351</fpage><pub-id pub-id-type="doi">10.2196/51351</pub-id><pub-id pub-id-type="medline">39393053</pub-id></nlm-citation></ref><ref id="ref19"><label>19</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Haupt</surname><given-names>F</given-names> </name><name name-style="western"><surname>Kanzow</surname><given-names>P</given-names> </name></person-group><article-title>The relation between students&#x2019; theoretical knowledge and practical skills in endodontics: retrospective analysis</article-title><source>Interact J Med Res</source><year>2023</year><month>04</month><day>18</day><volume>12</volume><fpage>e46305</fpage><pub-id pub-id-type="doi">10.2196/46305</pub-id><pub-id pub-id-type="medline">36994987</pub-id></nlm-citation></ref></ref-list><app-group><supplementary-material id="app1"><label>Multimedia Appendix 1</label><p>Sample size formula.</p><media xlink:href="resprot_v15i1e76783_app1.docx" xlink:title="DOCX File, 45 KB"/></supplementary-material></app-group></back></article>