Clinical Trial

Different Amounts of Moxibustion in the Treatment of DPN: A Clinical RCT Study

Active, Not Recruiting
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Record status
This record was last updated March 13, 2025 (before its estimated May 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to provide moxibustion treatment for diabetic peripheral neuropathy (DPN) and a reference for clinical treatment of DPN moxibustion. Patients will be randomly assigned to 3 clinical centers, 30 in each center, and then equally divided into 3 groups, including a drug treatment group, a 15-minute moxibustion group, and a 30-minute moxibustion group. Patients in the drug treatment group were given mecobalamin tablets and epalrestat at the same time of daily treatment (hypertension and hyperlipidemia combined with basic drug treatment) for 4 weeks. The frequency of moxibustion was 15/30 minutes per acupoint twice a week for 4 weeks. The results were evaluated during the baseline period (the day before the grouping), the treatment period (the end of the 8th treatment), and the follow-up period (a month after the end of treatment). The results of this part are expected to confirm the therapeutic effect of moxibustion on diabetic peripheral neuropathy. The results of this part will be expected to confirm the optimal amount of moxibustion in the treatment of diabetic peripheral neuralgia and provide a reference for the standardization of clinical treatment of moxibustion.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-03-25; most recent amendment 2025-03-10.
Status change: Not Yet Recruiting → Active, Not Recruiting 2025-03-10
Trial Details
NCT Number NCT06330233
Lead Sponsor Zhejiang Chinese Medical University
Collaborators: The First Affiliated Hospital of Zhejiang Chinese Medical University, Zhejiang Greentown Cardiovascular Hospital
Conditions Diabetic Peripheral Neuropathy, Pain, Moxibustion, Randomized Controlled Trial
Enrollment 90 participants
Start Date 2024-09-01
Primary Completion 2026-05-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-03-13