Skip to content

Moxibustion for Mild and Moderate Ulcerative Colitis

The Mechanism of Moxibustion in Treating Ulcerative Colitis Based on Metabonomics

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02084186
Enrollment
60
Registered
2014-03-11
Start date
2014-03-31
Completion date
2015-12-31
Last updated
2016-10-11

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

Conditions

Ulcerative Colitis

Brief summary

The purpose of this study is to determine whether moxibustion is effective to mild and moderate ulcerative colitis and the effect of moxibustion on metabolism.

Interventions

Ignited moxa cones are placed upon herbal cake. Herbs are smashed into powder. Every 2.8g medicine powder mix with 3g millet wine and then be pressed into herbal cakes which are 28mm in diameter and 7mm in high with a specific mould. Then the herbal cake with a moxa cone will be fixed on Tianshu and Shangjuxu.

OTHERbran-partitioned moxibustion

Ignited moxa cones are placed upon bran cake. Every 2.8g bran powder mix with 3g millet wine and then be pressed into bran cakes which are 28mm in diameter and 7mm in high with a specific mould. Then the bran cake with a moxa cone will be fixed on Tianshu and Shangjuxu.

Sponsors

Shanghai Institute of Acupuncture, Moxibustion and Meridian
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Meet the diagnosis of UC * Mayo ≤10 * Patients should have never received any pharmacological therapy or if they are receiving aminosalicylates and/or prednisolone (the dosage has been taken at least 4 weeks, and should be kept the same as before throughout the trial) * Patients should have never received antibiotic, biologicals, probiotics, acetaminophen, acetamide and contraceptive. * A written informed consent

Exclusion criteria

* Patients with cardiac, encephalic, hepatic, nephric, hematopoietic system, psychotic or any other serious diseases * Pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
disease activity index (DAI)3 monthsUsing Mayo subscore

Secondary

MeasureTime frameDescription
Inflammatory Bowel Disease Questionnaire (IBDQ)3 months
symptom score3 months
histomorphology observation of intestinal mucosa3 monthsUsing the Geboes histology score
metabolic profile of intestinal mucosa, urine, plasma and serum3 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026