This study will be a parallel-group, patient-blind, placebo-controlled RCT conducted in the Third Affiliated Hospital of Sun Yat-sen University, Ningxia Chinese Medicine Research Center, and the future Affiliated Hospital of Shanxi University of Traditional Chinese Medicine. The flowchart of this trial is shown in Figure 1. The trial consists of a 4-week treatment conducted along with a 3-month follow-up. After providing written informed consent, eligible participants will be randomized at a ratio of 1: 1 into one of 2 groups: an ACE group receiving ACE treatment or a sham ACE group receiving sham ACE treatments. Both groups will receive conventional loratadine treatment.

Participants will be recruited via advertisements, posters, leaflets about the trial, and doctor referrals from otorhinolaryngology clinics in the 3 study hospitals. Interested individuals will need to contact research assistants by phone or email. Trial information and consent forms will be sent to them to read before scheduling their first visit. In the first visit, screening evaluations will be conducted and recorded to ensure eligibility. For each participant who is eligible and willing to participate in the trial, research assistants will provide a signed consent form. The inclusion criteria for this trial are: (1) age between 18 and 65 years old; (2) meeting the diagnostic criteria for perennial AR; and (3) currently experiencing symptomatic attacks, able to accurately describe their condition, and willing to provide informed consent and participate in the clinical study.

Patients with AR were diagnosed based on the following criteria: (1) the presence of 2 or more symptoms including sneezing, clear watery nasal discharge, itchy nose, or nasal congestion that persists or occurs for more than 1 hour per day; (2) ocular symptoms such as itchy, watery, or red eyes; (3) nasal endoscopy showing pallor and edema of the nasal mucosa; and (4) a positive seasonal allergen test result for serum-specific IgE [18]. The exclusion criteria included: (1) recent respiratory infection or acute paranasal sinusitis within the past 14 days; (2) evidence of inflammation on chest X-ray; (3) history of chronic paranasal sinusitis or current diagnosis via X-ray examination; (4) the presence of organic lesions in the nasal cavity or recent nasal surgery; (5) diagnosis of paroxysmal respiratory diseases such as asthma; (6) recent use of H1-antihistamines, steroids, decongestants, or other medications affecting the respiratory system within the past 14 days; (7) specific immunotherapy or systemic hormone therapy within the last year; (8) recent use of acupuncture, moxibustion, cupping, nasal inhalation of traditional Chinese medicine, or other traditional therapies within the past 14 days; and (9) determination by clinical investigators that the patient is unable to adhere to the treatment regimen.

A block randomization sequence was generated by SAS software (version 9.2; SAS Institute Inc), which was performed by Guangdong Provincial Hospital of Chinese Medicine’s Key Unit of Methodology in Clinical Research. Eligible participants will be randomly assigned to either the ACE group or the sham ACE group at a ratio of 1:1. An independent researcher will prepare treatment cards, on which a serial number and one of 2 names are printed, each representing one of the 2 groups. This independent researcher will be responsible for selecting and adding intestinal thread to the injection needles according to the respective groups. Treatment allocations will be stored in password-protected files and held independently by staff of the Key Unit of Methodology in Clinical Research. While receiving the first treatment, the participants will be given sequential treatment cards from independent researchers to ensure adequate concealment. The participants will be allocated into one of 2 groups according to the name printed on their treatment card.

The researchers will assign intervention measures to the participants according to their allocated groups. The participants will be blinded to their group allocations in this single-blind study, whereas the researchers and acupuncturists will be aware of the group allocations. To minimize bias, outcome assessors will be blinded throughout the study.

A first-level blind base will be established for data statistics, ensuring the statistician is unaware of the group assignments. All operations will be performed in accordance with established standard operation procedures. After each treatment session, the participants in the ACE and sham ACE groups will complete a questionnaire on whether they believe they received ACE treatment and how certain they are that active treatment was received on a 0-to-10 numeric rating scale, where 10 represents absolute certainty [18]. Both the block randomization and the blinding questionnaire will be exclusively administered by a single external party.

To ensure operational consistency, all patients will receive unified treatment set by the same doctor. The research assistant will add intestinal threads to the injection needles according to the respective groups. The ACE group will undergo ACE. The bilateral YingXiang (LI20), QuChi (LI11), JianJing(GB21), YinTang(GV24+), and DanZhong (CV17) points will be disinfected. Detailed positioning data are shown in Table 1 and Figure 2. The patient will assume a supine position, and acupoints will be located, marked with a marker, and disinfected with iodophor cotton swabs.

The practitioner will wear aseptic gloves, cut the absorbable surgical suture around 5 mm, and place it into the front end of the needle tube. The structure of the acupuncture needle is illustrated in Figure 3. The doctor’s left thumb and index finger will tighten the skin around the operation site, and the needle will be inserted vertically with a catgut-burying needle in their right hand at a depth of 0.5 cm. The needle will be slightly lifted to stimulate the acupoints, and after getting qi, the left hand will push the needle core inward while the right hand withdraws the needle tube outward, embedding the surgical suture in the acupoint. After the stitches are placed, the pinhole will be pressed with aseptic gauze for a while and covered with a bandage or infusion paste.

Catguts will be implanted once every 7 days for a total of 28 days, and each participant will take a prescribed dose of loratadine orally every day. In the sham ACE group, participants will be placed in a supine position, and the acupoints will be located, marked with a marker, and disinfected with an iodophor cotton swab. The practitioner will wear sterile gloves and insert the needle into the skin. The doctor’s left thumb and index finger will tighten the skin around the operation site, and the needle will be inserted vertically with a catgut-burying needle in their right hand, at a depth of 0.5 cm. The needle will be slightly lifted to stimulate the acupoints, and after getting qi, the left hand will push the needle core inward. However, no absorbable surgical suture will be placed into the front end of the needle tube. After the procedure, the pinhole will be pressed with aseptic gauze for a while and covered with a bandage or infusion paste. This procedure will also be conducted once a week for 4 consecutive weeks. Each participant will take a prescribed dose of loratadine orally every day. Participants from both groups will be instructed to stop symptomatic RMs during the 1-week run-in and treatment periods. However, they will be allowed to take RMs if needed during the follow-up period. The use of RMs will need to be documented in the participants’ diaries.

For an evaluation of the primary and secondary outcome measures, the participants are required to complete 2 questionnaires, the Total Ocular Symptom Score (TOSS) and the Total Nasal Symptom Score (TNSS) [19]. These questionnaires will be completed at the beginning of each of the 4 treatment sessions (from week 2 to week 5) and in weeks 8, 12, and 16 during each follow-up session. During the follow-up process, the participants need to independently record their Rhinitis Control Assessment Test (RCAT) scores weekly [20]. In addition, the participants will be asked to complete diaries throughout the trial. The primary outcome is the recurrence rate 3 months after discontinuation. Once the treatment-effective participants discontinue the medication (RCAT score less than 21 points), they will immediately enter the follow-up period. If a relapse occurs, the relapse time will be promptly recorded, and the follow-up will conclude. Otherwise, the participants will continue to be monitored until 3 months after discontinuation of medication. RCAT is one of the most commonly used rhinitis control scales, and its reliability, validity, and responsiveness have been widely verified [21,22]. A score of 21 corresponds to the validated RCAT score of 25, which determines the controlled state of rhinitis. When RACT ≤21, it indicates an uncontrolled state of AR and the starting point for treatment [23]. RCAT is a simple self-rating scale that allows patients to assess their AR control at home and helps assess the success of long-term repeated treatment interventions [20,24]. TNSS evaluates 4 nasal symptoms: nasal obstruction, sneezing, rhinorrhea, and nasal itch. The symptoms are self-assessed and recorded by participants using a 5-point scale (0=no symptoms; 1=mild symptoms; 2=moderate symptoms; 3=severe symptoms; 4=very severe symptoms) [23]. TNSS scores range from 0 to 16, with low scores indicating lighter nasal symptoms. TOSS assesses eye symptoms, including redness, itchiness, and tearing. Each symptom is assessed on a scale between 0 and 3 (absent to most severe), with a total score from 0 to 9 [19,25]. The score represents an average for both eyes. The secondary outcomes include (1) changes in TNSS and TOSS score from baseline to weeks 8, 12, and 16; (2) response to interventions, defined as participants with a change in TNSS score of ≥0.5 from baseline; (3) and serum levels of tumor necrosis factor-alpha (TNF-α), IFN-γ, IL-4, IL-17, and IgE, measured by enzyme-linked immunosorbent assay according to the manufacturer's protocol (Bio-Techne).

The participants’ venous blood samples will be collected using blood collection tubes, symmetrically placed in the centrifuge sample bin, and covered. The rotation speed will be set to 4000 rpm, and the centrifuge time will be 10 minutes. The machine will be turned off after centrifugation, the sample bin opened, the sample carefully taken out, and the separation of the sample observed. If it is unsatisfactory, the sample will be centrifuged again. The serum will be carefully sucked from the upper layer with a 1-ml pipette, moved to an Eppendorf tube, and stored in a refrigerator at –80 °C degrees for inspection. Serum TNF-a, INF- γ, IL-17, IL-4, and IgE levels will be measured using enzyme-linked immunosorbent assay [26].

Demographics such as age, sex, height, body mass, and BMI will be obtained. Vital signs including temperature, blood pressure, heart rate, and breathing will also be measured. Data on patient medical history, family history, risk factors, and dietary history will be collected.

Intentional therapeutic analysis will be adopted, with missing values estimated using the last observation carried forward method. Mean and SD (for continuous variables that obey normal distribution), median and quartile (for continuous variables that do not obey normal distribution), and frequency and percentage (for classified variables) will be used for the statistical description. According to the numerical characteristics of the variables, quantitative data such as age, height, and weight of the 2 groups will be compared using a t test or the Wilcoxon rank sum test. The chi-square test or Fisher exact probability method will be used to compare qualitative variables, such as sex and nationality between the 2 groups. Cox regression analysis will be carried out with recurrence outcome and time of first recurrence as dependent variables, and the differences in survival curves between both groups will be compared. SPSS software (version 23.0; IBM Corp) will be used for statistical analysis. A 2-sided test will be used for all statistical inferences, and P<.05 will be considered statistically significant.

An independent data and safety monitoring committee evaluates the progress of the trial and assesses the safety data that may be requested during the trial. An adverse event (AE) is defined as any undesirable experience that participants undergo during the trial period, whether it is associated with the intervention or not. Participants will be instructed to report any AEs to the research team at any time. All details of AEs such as time of occurrence, severity, management, and causality to the intervention will be recorded on case report forms (CRFs). There are nine common AEs related to ACE: (1) lingering discomfort; (2) local hematoma or subcutaneous bleeding; (3) local swelling; (4) local induration; (5) severe pain; (6) thread extrusion; (7) local itching; (8) elevated body temperature after embedding the thread; and (9) local redness, swelling, heat, and pain after embedding the thread [27]. All AEs will be followed up from the date they are brought to the investigator’s attention until the AE is resolved. In the event of an emergency medical situation, the individual’s randomization code and group allocation will be identified via a standard operational procedure.

Before recruitment, the entire research team including acupuncturists, operational assistants, and research nurses were required to attend a training workshop. This was done before the trial to ensure their strict adherence to the study protocol and familiarity with the trial administration process. They were also provided with a written protocol and standard operation procedure documents. The 2 acupuncturists who will administer the treatment each have acupuncture licenses from the Chinese Ministry of Health and have over 5 years of experience in ACE application. The data collected in this trial comprise information recorded in CRFs and information on the RCAT, TNSS, TOSS, and blood routine examinations. Data will be entered using the double-entry method. The data quality will be checked regularly by research assistants and overseen by monitors. Data monitoring will be conducted regularly following standard operation procedures set by the Guangdong International Clinical Research Center of Chinese Medicine (Guangzhou, China). Audits will be performed regularly by the Department of Science Research at the Guangzhou University of Chinese Medicine. All modifications will be marked on the CRFs. Data managers will then recheck the data before logging them and promptly notify the research team if any discrepancy is found. The database will be locked after all data have been cleaned. If participants withdraw from the trial either during the treatment period or the follow-up phase, they are not required to provide any reasons. The withdrawal rate will be analyzed via statistics.

Our preliminary study [28] indicated that the 3-month recurrence rate of the ACE group should be at least 5% lower than that of the Sham ACE group to be clinically significant. Using α=0.025 (unilateral), β=0.2, △=5%, and K=1, the sample size was estimated based on the comparison of two sample rates in the optimization test. The sample size in each group was calculated to be 52. Since the effectiveness of any treatment was not 100%, patients with ineffective treatment in this study could not be included in the assessment of recurrence, so the loss of follow-up rate in this study was 20%, which amounted to 126 cases. The \following equation is used to calculate the sample size, which refers to the estimated number of patients to be enrolled in the study:

This study protocol has been approved by the Ethics Committee of the Guangzhou University of Chinese Medicine (B2014-014-01). It is explicitly outlined to all participants that the trial involves a waiting-list group and that informed consent to participate includes an agreement to undergo 3 months of clinical monitoring. All participants are provided with enough time to decide whether to sign the informed consent. This clinical study will adhere to the ethical principles outlined in the Declaration of Helsinki (2024) and relevant national regulations. Prior to study initiation, the trial protocol underwent rigorous review and approval by the Ethics Committee of Ningxia Medical University (2024-075). Written informed consent must be obtained from each participant before randomization.