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Symptom management for irritable bowel syndrome

Symptom management for irritable bowel syndrome : a pilot randomized controlled trial of moxibustion.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002064
Enrollment
24
Registered
2016-09-19
Start date
2016-10-04
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

None listed

Interventions

Procedure/Surgery : Intervention group : Subjects were blind-folded, then moxibustion intervention will be applied to Guan Yuan(CV4) using 5 moxibustion plates for 20 minutes. At the same time, infra-

Sponsors

Semyung University Oriental Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) between 18 years and 30 years man and woman (2) repeated abdominal pain or discomfort(an uncomfortable sensation not described as pain) at least 3 times per month (3) associated with two or more of the following recent 3 months (a) Improvement with defecation (b) Onset associated with a change in frequency of stool (c) Onset associated with a change in form (appearance) of stool (4) 1 )Bristol Stool Chart Scale 6-7)?25% 2) Bristol Stool Chart Scale 1-2.)?25% (5) if women, negative in urine pregnancy test and agree with not being pregnant during clinical trial (6) not diagnosed with cardiovascular disease like hypertension, diabetes mellitus, hyperlipidemia (7) recently body temperature not being over 38.5 celsius lasting at least 4 hours (8) those who sign in IRB approved consent and agree with clinical trial plan and follow-up observation

Exclusion criteria

Exclusion criteria: (1) Diagnosed with cardiovascular disease (2) had high fever in recent 1 week (3) before clinical trial screening process, if the subject was participated in other clinical trial and administered medication(include placebo) for clinical trial in recent 30days. (4) considered as inappropriate subject by clinical trial researcher.

Design outcomes

Primary

MeasureTime frame
Bowel Symptom Severity Scale(BSSS) score

Secondary

MeasureTime frame
Irritable Bowel Syndrome Severity Scale–Korean Version ; temperature difference between Dan Zhong(CV17) and Chung-wan(CV12);Cold-Heat Pattern Questionnaire Score; Qi-stagnation questionnaire score,; visceral sensitivity Questionnaire score;Heart Rate Variability

Countries

Korea, Republic of

Contacts

Public ContactSeon Mi Shin

Semyung University

bunggujy21@hanmail.net+82-43-649-1873

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026