Efficacy of Treatment With Berberine to Maintain Remission in Ulcerative Colitis

Sponsor
Xijing Hospital of Digestive Diseases (Other)
Overall Status
Unknown status
CT.gov ID
NCT02962245
Collaborator
(none)
238
2

Study Details

Study Description

Brief Summary

The research aim to find out whether berberine can reduce the annual recurrence rate of ulcerative colitis in remission.

A total of 238 patients with ulcerative colitis in remission will be randomly divided into two groups.One will receive regular treatment,and the other group will receive extra oral berberine 300 mg three times daily for a year.

The end of the study for every patient is disease recurrence(Mayo Clinic score of 3 points or more ).

The primary analysis is annual recurrence rate, and both endoscopy and Mayo Clinic disease activity index scores at the baseline and final assessments.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
238 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Treatment With Berberine to Maintain Remission in Ulcerative Colitis: An Open-label,Randomized,Phase IV Clinical Trial
Study Start Date :
Nov 1, 2016
Anticipated Primary Completion Date :
Jan 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: berberine group

regular treatment and receive oral berberine 300mg three times daily untill recurrence in one year

Drug: berberine

Drug: regular treatment
such as 5-ASA,immunomodulating/suppressive agents or Anti-TNF therapy

Placebo Comparator: regular treatment group

regular treatment untill recurrence in one year

Drug: regular treatment
such as 5-ASA,immunomodulating/suppressive agents or Anti-TNF therapy

Outcome Measures

Primary Outcome Measures

  1. Annual Recurrence Rate [a year]

Secondary Outcome Measures

  1. Disease exacerbation rate measured by Mayo Clinic disease activity index scores [a year]

    The primary analysis is disease exacerbation through day 14 among patients who underwent randomization, had Mayo Clinic disease activity index scores at the baseline and final assessments. Disease exacerbation is defined as a total Mayo Clinic score of 5 points or more and an increase in the endoscopic score of 1 point or more.

  2. Number of participants with treatment-related adverse events as assessed by CTCAE v4.03 [a year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Diagnosis with ulcerative colitis(according to the second European evidence-based consensus on the diagnosis and management of ulcerative colitis);

  2. Disease remission of ulcerative colitis(a total Mayo Clinic score of 2 points or less and an endoscopic score of 1 point or less);

  3. Diagnosis of moderate or severe ulcerative colitis within 3 months(a total Mayo Clinic score of 6-12 points)

Exclusion Criteria:
  1. Prior bowel resection surgery;

  2. Women who are planning or actual pregnancy or lactation during study period;

  3. Patients allergic to berberine;

  4. History of disease that would interfere with their participation in the trial, including malignant diseases, bleeding disorders, active gastric or active duodenal ulcers, autoimmune diseases, and mental or emotional disorder;

  5. Take the following treatment:

  • Unstable dose of 5-ASA drugs (oral and/or rectal route) within 14 days prior to screening;

  • Unstable dose of any immunomodulating/suppressive agents and any Anti-TNF therapy within 3 months prior to screening;

  • Traditional Chinese Medicine for the treatment of UC (any pharmaceutical form) within 7 days prior to screening.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Xijing Hospital of Digestive Diseases

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yongquan Shi, professor, Xijing Hospital of Digestive Diseases
ClinicalTrials.gov Identifier:
NCT02962245
Other Study ID Numbers:
  • KY20162062-1
First Posted:
Nov 11, 2016
Last Update Posted:
Nov 11, 2016
Last Verified:
Nov 1, 2016
Keywords provided by Yongquan Shi, professor, Xijing Hospital of Digestive Diseases
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 11, 2016