Transfer of Feces in Ulcerative Colitis 2; Improving Efficacy

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this placebo-controlled randomised multicenter trial is to evaluate the efficacy and safety of anaerobic prepared donor fecal microbiota transplantation (FMT) compared to autologous FMT in patient with ulcerative colitis. Participants will receive 4 treatments with frozen FMT via both upper and lower gastro-intestinal route (infusion via duodenal tube and enemas). Donors are selected based on microbiota profile.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

• Age ≥18 and \<70

• Ability to give informed consent

• Established ulcerative colitis with known involvement of the left colon according to the Lennard-Jones criteria

• Partial mayo score of ≥ 3 and calprotectin \> 250

• Full Mayo score 5-9

• Endoscopic Mayo score of ≥2 in either the rectum or sigmoid upon screening sigmoidoscopy

• Stable dose of thiopurines or , 5-ASA, or budesonide in preceding 8 weeks.

• Stable dose of budesonide in preceding 2 weeks.

• Prednisone use ≤15mg/day in preceding 2 weeks with a mandatory taper of 5 mg per week starting from week 4.

• Women need to use reliable contraceptives during participation in the study

• Alkaline phosphatase \> 1.5 x ULN in the subgroup of PSC/UC patients.

Locations
Other Locations
Netherlands
Amsterdam University Medical Center
RECRUITING
Amsterdam
Contact Information
Primary
Cyriel Ponsioen, prof.
c.y.ponsioen@amsterdamumc.nl
+31 20 5668278
Backup
Melanie Benard, Msc
m.v.benard@amsterdamumc.nl
0031645050314
Time Frame
Start Date: 2018-12-05
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 76
Treatments
Experimental: Donor fecal microbiota transplant
Placebo_comparator: Autologous fecal microbiota transplant
Sponsors
Collaborators: UMC Utrecht, University Medical Center Groningen
Leads: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

This content was sourced from clinicaltrials.gov

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