Trial of Mesalamine for the Treatment of Active Microscopic Colitis

Last updated: May 20, 2011
Sponsor: Mayo Clinic
Overall Status: Completed

Phase

2/3

Condition

Colic

Stomach Discomfort

Bowel Dysfunction

Treatment

N/A

Clinical Study ID

NCT00952952
06-003637
evans 06
  • Ages > 18
  • All Genders

Study Summary

Subjects must be 18 years old and older, have diarrhea and microscopic colitis. Pregnant or nursing females are excluded. They can't have other untreated diarrheal conditions. Subjects will receive medication for 8 weeks, followed by sigmoidoscopy with biopsies. The subjects will be monitored weekly. A pathologist will review pre and post treatment biopsies. Subjects that show improvement will be followed for 4 weeks post medication.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Subjects must be 18 years old and older.

  • Have diarrhea and microscopic colitis.

  • They need to have a colon biopsy done at the Mayo Clinic in Rochester, MN within ayear of enrollment.

Exclusion

Exclusion Criteria:

Study Design

Total Participants: 70
Study Start date:
February 01, 2007
Estimated Completion Date:
November 30, 2007

Study Description

We propose a prospective, randomized trial of mesalamine at 1.2g and 4.8g doses for the treatment of microscopic colitis. Our hypothesis is mesalamine is safe and effective for the treatment of diarrhea in microscopic colitis and that the 4.8g dose is more effective than the 1.2g dose.

We will recruit 70 subjects. The subjects will be randomized into to two groups, 4.8g dose, and 1.2g dose groups. Subjects will receive medication for 8 weeks, followed by sigmoidoscopy with biopsies. The subjects will be monitored weekly. A pathologist will review pre and post treatment biopsies. Responders will be followed for 4 weeks post medication.

Subjects must be 18 years old and older, have diarrhea and microscopic colitis. Subjects will be excluded if they have unsuccessful treatment or side effects to 5-ASA drugs, oral corticosteroids, or salicylate. and antibiotics, mesalamine, bismuth or steroid use in the last two weeks. Subjects may not be on anticholinergics, cholestyramine, digoxin. Pregnant or nursing females are excluded. They can't have other untreated diarrheal conditions.

A two-sample z-score test for proportions will be used to test whether relief rates are different between groups.

Connect with a study center

  • Mayo Clinic

    Rochester, Minnesota 55905
    United States

    Site Not Available

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