Clinical Trials Directory

Trials / Completed

CompletedNCT02421627

Moxibustion for Diarrhea-predominant Irritable Bowel Syndrome

Study on the Mechanism of Moxibustion Effect on Treating Diarrhea-predominant Irritable Bowel Syndrome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Shanghai Institute of Acupuncture, Moxibustion and Meridian · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

To observe the safety and efficacy of moxibustion on diarrhea-predominant irritable bowel syndrome and evaluation by Magnetic Resonance Imaging (MRI), Event related potential (ERP).

Detailed description

1. A randomized controlled trial 2. Moxibustion treatment, sham control 3. To observe the safety and efficacy of moxibustion treatment versus placebo control 4. Evaluation by intestinal microbial structural and diversity changes using 16S rDNA sequencing 5. Evaluation by structural MRI and resting state-functional MRI 6. Evaluation by ERP

Conditions

Interventions

TypeNameDescription
DEVICEmoxibustionAcupoints: Tianshu (ST25,bilateral), Zusanli (ST36,bilateral). using mild-warm moxibustion,the surface temperature of acupoints were maintained at 43 ℃ ± 1 ℃, 30min for each acupoint, once every other day, three times a week, a total of six weeks treatment. After the treatment, subjects were followed up at weeks 12, 18 and 24.
DEVICESham moxibustionAcupoints: Tianshu (ST25,bilateral), Zusanli (ST36,bilateral); using sham mild-warm moxibustion,the surface temperature of acupoints were maintained at 37 ℃ ± 1 ℃, 30min for each acupoint, once every other day, three times a week, a total of six weeks treatment. After the treatment, subjects were followed up at weeks 12, 18 and 24.

Timeline

Start date
2015-04-01
Primary completion
2018-12-31
Completion
2018-12-31
First posted
2015-04-20
Last updated
2020-02-10

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT02421627. Inclusion in this directory is not an endorsement.