Fecal Microbiota Transplantation in Crohn's Disease as Relay After Anti-TNF Withdrawal
MIRACLE
2 other identifiers
interventional
150
1 country
1
Brief Summary
Crohn's disease (CD) is a chronic inflammatory bowel disease. CD pathogenesis remains poorly understood but involves an inappropriate immune response toward an unbalanced gut microbiota in predisposed hosts. The purpose of this study is to evaluate de clinical efficacy of the fecal microbiota transplantation (FMT) as a maintenance treatment following anti-TNF agent withdrawal in CD's patient.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_3
Started Sep 2021
Longer than P75 for phase_3
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 5, 2021
CompletedFirst Posted
Study publicly available on registry
August 10, 2021
CompletedStudy Start
First participant enrolled
September 22, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 22, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 22, 2029
August 11, 2025
August 1, 2025
5.7 years
July 5, 2021
August 6, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Evaluate the clinical efficacy of FMT versus sham transplantation as a maintenance treatment following anti-TNF agent withdrawal in patients with Crohn's disease in steroid-free clinical remission for at least 6 months under anti-TNF agent
Clinical remission (defined by a Crohn's disease activity index (CDAI) \<150) at week 52 (V8) without any flare between week 0 (colonoscopy (V2)) and week 52 (V8). Flare is defined by a CDAI (Addendum 2) above 250 or between 150 points and 250 points with a 70-point increase from baseline over 2 consecutive weeks and the need
52 weeks after FMT or sham-transplantation
Secondary Outcomes (1)
Relapse free survival
52 weeks after FMT or sham-transplantation
Other Outcomes (7)
Mucosal healing
52 weeks after FMT or sham-transplantation
Clinical remission
52 weeks after FMT or sham-transplantation
Endoscopic remission
52 weeks after FMT or sham-transplantation
- +4 more other outcomes
Study Arms (2)
Fecal microbiota
EXPERIMENTALPatients receiving the fecal microbiota transplantation (FMT) in 3 times after inclusion and randomisation (endoscopic and oral)
Sham-transplantation
SHAM COMPARATORPatients receiving the sham-transplantation in 3 times after inclusion and randomisation (endoscopic and oral)
Interventions
The colonoscopy for FMT will be planned between 7 and 14 days after the last adalimumab or sub-cutaneous infliximab administration and 6 weeks +/- 7 days after the last intravenous infliximab administration 14 and 28 days following the last sub-cutaneous golimumab administration. After colon cleansing using polyethylene glycol, the patient will have a colonoscopy under general anesthesia. The patient will then receive either FMT (frozen preparation of 50g of stools in 300ml of saline (NaCl 0.9%), (FMT vehicle in the terminal ileum or the colon. At W12 and W24 after first colonoscopy, the patient receives treatment by capsule (15 capsules contain 0.8g of stools by visit).
The colonoscopy for sham-transplantation will be planned between 7 and 14 days after the last adalimumab or sub-cutaneous infliximab administration and 6 weeks +/- 7 days after the last intravenous infliximab administration, 14 and 28 days following the last sub-cutaneous golimumab administration. After colon cleansing using polyethylene glycol, the patient will have a colonoscopy under general anesthesia. The patient will then receive either sham transplantation (frozen preparation of NaCl 0.9% with 10% glycerol) in the terminal ileum or the colon. At S12 and S24 after first colonoscopy, the patient receives treatment by capsule (15 capsules contain placebo).
Eligibility Criteria
You may qualify if:
- Age ≥ 18 years and \< 75 years
- Crohn's disease (according to the Lennard-Jones criteria) for at least 6 months
- Female of child-bearing age with an active contraception and this during at least the period of treatment (week 52)
- Patient with health insurance
- Informed Written consent
- Age ≥ 18 years and \< 50 years
- kg/m² \< body mass index \< 30 kg/m²
- Regular bowel movement defined as at least 1 stool every other day and maximum 2 stools per day
- Subject with health insurance (AME excepted)
- Informed written consent
You may not qualify if:
- Crohn's Disease complication requiring surgical treatment
- Contraindication to colonoscopy or anesthesia
- Pregnancy or breastfeeding during the study (Cf. Addendum 4)
- Diagnosis of Crohn's disease restricted to the upper gastrointestinal tract (oesophagus, stomach, duodenum, jejunum)
- Patient with active perineal disease (defined as evidence of perineal abscess or active draining fistula or presence of seton or presence of perineal ulceration)
- History of more than one small bowel resection or small intestine resection \> 1 meter
- Participation in any other interventional study
- Patient under legal protection
- \- For details, please see protocol
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Assistance Publique - Hôpitaux de Parislead
- CRB-HUEPcollaborator
- Institut National de la Santé Et de la Recherche Médicale, Francecollaborator
Study Sites (1)
Gastroenterology Department of Saint Antoine Hospital
Paris, 75012, France
Related Publications (34)
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Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Harry SOKOL, PU-PH
Assistance Publique - Hôpitaux de Paris
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 5, 2021
First Posted
August 10, 2021
Study Start
September 22, 2021
Primary Completion (Estimated)
May 22, 2027
Study Completion (Estimated)
July 22, 2029
Last Updated
August 11, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share