Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04401605

Fermented Food-Supplemented Diet in Ulcerative Colitis

Led by Stanford University · Updated on 2026-02-27

21

Participants Needed

1

Research Sites

350 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to see how a diet that supplements fermented foods effects inflammation and quality of life in patients with mild to moderate Ulcerative Colitis (UC). There is a paucity of research and an enormous need for better understanding of diet and intestinal inflammation. Fermented food have been shown to positively influence inflammatory cytokines and intestinal microbial diversity in healthy volunteers.

CONDITIONS

Official Title

Fermented Food-Supplemented Diet in Ulcerative Colitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent
  • Male or female subjects, 18 years of age or older
  • Confirmed diagnosis of Ulcerative Colitis
  • Symptomatic disease defined as partial Mayo Score 2 to 7 (inclusive)
  • Elevated fecal calprotectin
Not Eligible

You will not qualify if you...

  • Women who are pregnant, nursing, or expect to be pregnant
  • Intolerance to fermented food
  • Individuals with a body mass index (BMI) lower than 18
  • Individuals diagnosed with a serious medical condition unless approved in writing by a physician
  • Individuals who have been severely weakened by a disease or medical procedure
  • Individuals with more than mild-moderate cardiovascular disease or life-threatening cancer unless approved by a physician
  • Individuals with history of severe cardiac disease such as uncompensated congestive heart failure NYHA grade 2 or more or LVEF less than 40%
  • History of relevant intestinal surgery such as total or hemi-colectomy, proctocolectomy, or stoma

AI-Screening

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Trial Site Locations

Total: 1 location

1

Stanford University

Palo Alto, California, United States, 94305

Actively Recruiting

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Research Team

T

Touran Fardeen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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