About this trial
This study included two topics: one was to test the efficacy and safety of fecal microbiota transplants plus partial enteral nutrition (PEN) in refractory pediatric UC where conventional therapy has failed, and the other was to explore the efficacy and safety of FMT plus PEN as first-line therapy for pediatric active UC
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Single group
Treatments tested in this trial
Fecal Microbiota Transplantation
Other interventionIn the induction stage of UC, FMT group received FMT and PEN intervention, and FMT group are given for at least one course of FMT treatment. If repeated FMTs are received, it is usually at a 2 month interval. All the participants received PEN (80% of total calories as a polymeric diet, Peptamen, Nestle, Vevey, and Switzerland) intervention to help induce and maintain clinical remission.
Treatment groups
Trial outcomes
Primary outcomes
clinical response
reduction in the Pediatric Ulcerative Colitis Activity Index (PUCAI) ≥30% from baseline
clinical remission
Clinical remission defined as a PUCAI \<10
safety of FMT
All possible adverse events: fever, abdominal pain, infectious diseases and others.
Secondary outcomes
Number of patients requiring escalation of medical therapies
Number of patients requiring escalation of medical therapies based on clinical relapse. Clinical relapse is defined by requiring additional medical therapy.
Number of patients with endoscopic remission
Number of patients with endoscopic remission as defined by a PUCAI score of 0
Fecal calprotectin level
Mean change of Fecal calprotectin levels
C-reactive protein levels
Mean change of C-reactive protein levels
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Biao Zou
Lead sponsor
Tongji Hospital
Sponsor institution