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CompletedNCT01972906

Moxibustion for Primary Dysmenorrhea

Traditional Chinese Moxibustion for Primary Dysmenorrhea

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
152 (actual)
Sponsor
Chengdu University of Traditional Chinese Medicine · Academic / Other
Sex
Female
Age
13 Years – 35 Years
Healthy volunteers
Not accepted

Summary

Hypothesis: Moxibustion is effective for managing primary dysmenorrhea. Aim: To attest the effectiveness and safety of moxibustion for primary dysmenorrhea. Design: A randomized controlled trial. 152 participants will be included. Two arms: moxibustion treatment group and ibuprofen control group.

Detailed description

There is no convincing evidence for the efficacy of moxibustion for primary dysmenorrhea, due to low methodologic quality and small sample size. The investigators designed the random clinical trial to investigates the effectiveness of moxibustion in treating primary dysmenorrhea, the purpose of this study is to provide the research base of moxibustion efficacy. The investigators also examined the acceptability and any adverse effects associated with the use of moxibustion.

Conditions

Interventions

TypeNameDescription
DEVICEmoxibustionapply moxibustion according to traditional Chinese medicine
DRUGIbuprofen Sustained Release Capsulesapply Ibuprofen (H20013062), 0.3g, Bid, lasting 3 days before menstrual cycle

Timeline

Start date
2012-02-01
Primary completion
2014-02-01
Completion
2014-06-01
First posted
2013-10-31
Last updated
2014-12-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01972906. Inclusion in this directory is not an endorsement.

Moxibustion for Primary Dysmenorrhea (NCT01972906) · Clinical Trials Directory