Skip to content

Moxibustion for alleviating abdominal pain and distension in IBS-D patients: a randomized, controlled trial

Moxibustion for alleviating abdominal pain and distension in IBS-D patients: a randomized, controlled trial

Status
Unknown
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230112006
Enrollment
164
Registered
2023-01-12
Start date
2023-02-07
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diarrhea irritable bowel syndrome (IBS-D) was the most common subtype in China, and currently there was no effective cure. Moxibustion plays an important role in the traditional medical systems of China, and it has been promoted for a wide variety of conditions, such as urinary retention, pain, cancer, stroke, constipation, and hypertension. However, most researches of moxibustion on IBS were generally of low quality and the application of moxibustion still lack of high quality evidence. We cond

Interventions

Patients in the treatment group were treated by moxibustion therapy once every other day, 3 times a week for 6 weeks in total. Moxa rolls provided by Nanyang Chinese Medicine Airong Co. LTD (Henan, C
Experimental Other
moxibustion therapy

Sponsors

Meiya Xu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1)met the Rome III diagnostic criteria and Bristol Form Scale for IBS-C; 2)were 18-65 years old; 3) had IBS-D for more than 6 months; 4) had a baseline IBS-Symptom Severity Score (IBS-SSS) of 75 or higher; 5)were with signed informed consent.

Exclusion criteria

Exclusion criteria: 1)were accompanied with inflammatory bowel disease, intestinal organic lesions, peptic ulcer, infectious diarrhea; 2) were accompanied with serious cardiovascular or cerebrovascular diseases, or severe liver or kidney dysfunction; 3) were pregnant or had reproductive plan within 1 month; 4) had participated in other clinical trials 1 month before.

Design outcomes

Primary

MeasureTime frame
IBS-SSS from week 0 to week 6 6 weeks changes in total IBS-SSS from week 0 to week 6

Secondary

MeasureTime frame
IBS-SSS from week 6 to week 18 18 weeks changes in total IBS-SSS from week 6 to week 18

Countries

China

Contacts

Public ContactMeiya Xu

Changshu Hospital Affiliated to Nanjing University of Chinese Medicine

CSSZYYXMY@163.com18032601285

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026