drugset / Trial / NCT02255305

FMT Versus Antimicrobials for Initial Treatment of Recurrent CDI

NCT02255305 ↗

Phase 2 Terminated 6 enrolled Endeavor Health
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to determine the safety and efficacy of Fecal Microbiota Transplant (FMT) for the treatment of the recurrence of Clostridium difficile infection (CDI) as compared to standard antibiotic therapy. Patients who have tested positive for CDI within 90 days of an admission for relapse of CDI will be approached to participate in this open-label, randomized controlled trial. Patients will either be randomized to the intervention group (receive FMT via retention enema) or the control group (receive antimicrobials targeting CDI).

Timeline

Start
2015-01
Primary completion
2020-01
Completion
2020-01

Outcome

Outcome not reported

Stopped (Enrollment): “Due to personnel issues for finding and enrolling patients, performing appropriate follow-up and performing FMT procedure”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fecal Microbiota Transplant Other / unclassified 50 g Rectal