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Ancient heat therapy targets gut bugs to ease IBS
NCT ID NCT07308262
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a traditional Chinese therapy called umbilical moxibustion (applying heat near the belly button) can help people with irritable bowel syndrome (IBS). Researchers will compare gut bacteria and blood chemicals between 60 patients who receive the therapy and those who don't. The goal is to understand how this treatment might work, not to prove it cures IBS.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- umbilical moxibustion (a traditional Chinese therapy involving heat at the belly button)
- What this could lead to
- If successful, this could reveal how moxibustion changes gut bacteria and metabolites, pointing toward a better understanding of IBS treatment.
- What could go wrong
- This is a very small, early study (60 people) focused on understanding mechanisms, not proving a cure. It may not lead to a new treatment, and results may not apply to all IBS patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Sample Size: 60 cases (30 in the umbilical moxibustion group, 30 in the control group), determined using G\*Power (effect size d = 0.8, α = 0.05, β = 0.2; with a minimum of 26 cases per group, 15% attrition rate reserved, final 30 cases per group). Grouping Method: A random number table generated by SPSS 26.0 was used to allocate participants in a 1:1 ratio, with sealed envelopes employed to conceal group assignments.
- Ages
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18 to 65 years
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Study Type: Prospective, single-blinded, randomized controlled trial (patient-blinded, researcher-unblinded).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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