Immunonutrition in Ulcerative Colitis

Last updated: July 11, 2018
Sponsor: Baptist Memorial Health Care Corporation
Overall Status: Active - Recruiting

Phase

N/A

Condition

Colic

Ulcerative Colitis

Inflammatory Bowel Disease

Treatment

N/A

Clinical Study ID

NCT03594708
UCS2018
  • Ages > 18
  • All Genders

Study Summary

This study tests the hypothesis that a supplement that combines a functional fiber, long chain omega-3 polyunsaturated fatty acids (PUFAs), vitamin D3, vitamin E, and zinc will reduce clinical symptoms, decrease pro-inflammatory cytokines in the blood and ergo decrease inflammation, promote beneficial microbial activity in the colon, and help recovery of the intestinal mucosa of ulcerative colitis (UC) patients compared with a placebo.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • patients with active ulcerative colitis (proof of diagnosis from gastroenterologist),over 18 years old, has over 50% gut remaining, fully connected bowels (no colostomy),currently on 5-aminosalicylates (ASA) drugs, not pregnant or lactating

Exclusion

Exclusion Criteria:

Study Design

Total Participants: 30
Study Start date:
April 30, 2018
Estimated Completion Date:
December 31, 2018

Study Description

An anticipated 30 participants with newly diagnosed active ulcerative colitis will be recruited to participate in a randomized control trial, with 50% of the subjects distributed to the supplement (n=15) and the other 50% provided a placebo control (n=15). This is considered as a "proof of concept" study to determine if there is evidence that a multi-ingredient supplement (immunonutrition) will reduce UC disease severity.

Connect with a study center

  • GI Specialists Foundation

    Memphis, Tennessee 38120
    United States

    Active - Recruiting

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