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Completed

NCT Number: NCT03078803

Fecal Transplant for Crohn's Disease

To determine the efficacy and safety of serial FMT at inducing and maintaining clinical and endoscopic response in patients with mild to moderate Crohn's disease

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Foothills Hospital, Calgary, Alberta, Canada

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About this study

Double blind study will randomize patients with mild to moderate Crohn's 1:1 (FMT : water) stratified by disease duration and current use of biologic therapy. First FMT/placebo at week 0 by colonoscopy plus weekly FMT/placebo by capsules for 7 weeks. At week 8, a repeat colonoscopy will be done and endoscopy score repeated.

Responders in FMT arm are eligible to enter open label phase to receive FMT by capsules q2 weeks.

Blood, stool and urine samples, colonic biopsies will be collected. Quality of Life as measured by Short Inflammatory Bowel Disease Questionnaire, EuroQol five dimensions, and Work Productivity and Activity Impairment Questionnaire: Crohns disease and dietary intake diary collected.

Colonoscopies recorded and reviewed by a central reader.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • mild to moderate ileal, ileo-colonic or colonic Crohns disease
  • active ileal and/or colonic disease on endoscopy with or without elevated inflammatory markers i.e. C-reactive protein >8mg/L, elevated fecal calprotectin >250 ug/g
  • If applicable, meds stable as follows: 5-ASA for 4 weeks, prednisone up to 20mg QD for 4 weeks, budesonide up to 6mg QD for 4 weeks, azathioprine, 6-MP and methotrexate for 12 weeks
  • Use of effective contraception

Exclusion criteria

  • Antibiotic exposure within 30 days and probiotic exposure within 14 days
  • topical inflammatory bowel disease therapy within 2 weeks
  • active perianal disease
  • requirement for concurrent antibiotic therapy
  • SES-CD score <5
  • severe CD HBI >25 or need for hospitalization
  • abdominal abscess
  • extensive colonic resection, subtotal or total colectomy
  • ileostomy, colostomy, known fixed symptomatic stenosis or complex fistulae
  • evidence of or treatment for C. difficile or other intestinal pathogen including Cytomegalovirus within 28 days
  • requiring or expected to require surgical intervention
  • history or evidence of adenomatous colonic polyps not removed
  • history of evidence of colonic dysplasia
  • active substance abuse or psychiatric problems that may interfere with study
  • chronic Hep B, C, or HIV infection
  • pregnancy or planning to become pregnant
  • upper CD
  • history of adhesions preventing colonoscopy to cecum
  • planned bowel resection within 3 mon of enrollment

Treatment and study plan

Fecal Microbiota Transplant (FMT)

Biological

FMT delivered by colonoscopy and oral capsules

Other names: FMT

Placebo

Biological

Transfer of water only

Primary outcomes

  1. Clinical and Endoscopic Remission

    Time frame: Week 8

    Harvey Bradshaw Index <5 and Simple endoscopic score <5

Secondary outcomes

  1. Clinical response

    Time frame: Week 8

    Harvey Bradshaw Index reduction by 3 points

  2. Clinical remission

    Time frame: Week 8

    Harvey Bradshaw Index <5

  3. Endoscopic response

    Time frame: Week 8

    Simple endoscopic score reduction by 50%

  4. Endoscopic remission

    Time frame: Week 8

    Simple endoscopic score <5

  5. Quality of Life 1

    Time frame: Week 8

    Mean changes in Short Inflammatory Bowel Disease Questionnaire

  6. Quality of Life 2

    Time frame: Week 8

    Mean changes in Euro five dimensions questionnaire

  7. Quality of Life 3

    Time frame: Week 8

    Mean changes in Work Productivity and Activity Impairment: Crohns Disease questionnaire

Sponsors and collaborators

Lead sponsor

University of Alberta

Other

Collaborators

  • McMaster University
  • University of Calgary

Registry information

Official study title

A Prospective Multicenter Randomized Controlled Trial Comparing Fecal Microbiota Transplantation (FMT) to Placebo in the Treatment of Mild to Moderate Crohn's Disease

Important dates

Study start
2017
Primary completion
2021
Study completion
2022
First posted
Mar 13, 2017
Registry last updated
Sep 7, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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