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COMPLETED
NCT07799285
NA

Suspended Moxibustion for Primary Dysmenorrhea in Female Medical Students

Sponsor: Can Tho University of Medicine and Pharmacy

View on ClinicalTrials.gov

Summary

This study evaluates the analgesic efficacy of suspended moxibustion applied at acupoints CV4 (Guanyuan), CV8 (Shenque), and bilateral SP6 (Sanyinjiao) in female students with primary dysmenorrhea at Can Tho University of Medicine and Pharmacy. In this single-arm pre-post clinical intervention (N=48), participants received daily 20-minute moxibustion sessions starting 7 days before menstruation through the end of the menstrual period, across three consecutive treatment cycles. The primary outcome was change in VAS pain score; secondary outcomes included RSS-COX symptom burden, number of pain days per cycle, and abdominal skin temperature measured by thermal imaging (FLIR C5).

Official title: Evaluating the Analgesic Efficacy of Suspended Moxibustion in the Treatment of Primary Dysmenorrhea in Female Students at Can Tho University of Medicine and Pharmacy

Key Details

Gender

FEMALE

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2025-12-01

Completion Date

2026-07-20

Last Updated

2026-09-02

Healthy Volunteers

Yes

Interventions

OTHER

Suspended moxibustion at CV4, CV8, SP6

Moxa stick suspended 2-3 cm above the skin at acupoints CV4 (Guanyuan), CV8 (Shenque), and bilateral SP6 (Sanyinjiao), targeting a skin temperature of 40-45°C, administered once daily for 20 minutes p

Locations (1)

Can Tho University of Medicine and Pharmacy

Can Tho, Ninh Kieu, Vietnam