Safety Registry of a Fecal Microbiota Transplant Cohort

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Clostridium difficile infection (CDI) is a major cause of infectious diarrhea and the most important cause of nosocomial diarrhea. Recurrent forms are a major problem with this infection. The use of fecal microbiota transplantation (FMT), FMT appears in the most recent European and North American recommendations.

There is no cohort or multicenter registry in France prospectively collecting FMTs, the methods used, their efficacy and side effects. Likewise, there is no prospective collection focused on the cohort of stool donors. A large national cohort of patients who have undergone FMT as part of routine care as well as donors, is essential for evaluating the safety of FMT.

Eligibility criteria

Qualifiers

Adult patient with an indication for FMT for CDI (severe refractory CDI, recurrent CDI);

Informed written consent

Adult (18 years or older)

Informed Written consent

Disqualifiers

insufficient level of understanding of written and spoken French language

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

305 Participants
are grouped into 2 trial groups