drugset / Trial / NCT07454408

Evaluation of the Outcome of Fecal Microbiota Transplantation

NCT07454408

Phase 1/2 Not yet recruiting 40 enrolled Air Force Military Medical University, China
RandomizedParallel-groupDouble-blindPrevention

Summary

This study is a randomized, placebo-controlled, exploratory phase II clinical trial led by Professor Han Gyeong-ho from the Digestive Disease Hospital of Xi'an International Medical Center. The study enrolled 40 patients who had experienced recurrence of hepatic encephalopathy despite treatment with rifaximin and lactulose. These patients were randomly divided 1:1 into the experimental group and the control group. After obtaining informed consent from the patients, fecal microbiota transplantation or placebo control was performed. The fecal microbiota was sourced from the feces of healthy individuals who had a rich composition of the Muribaculaceae, Ruminococcaceae, and Bifidobacteriaceae families and did not contain pathogenic bacteria. The safety and efficacy of the treatment were followed up, and blood and fecal samples were collected for sequencing analysis. The aim was to provide new solutions for patients with hepatic encephalopathy who did not respond to the treatment with rifaximin and lactulose after TIPS surgery; and to explore the impact of microbiota changes and translocation on the recurrence of hepatic encephalopathy after TIPS surgery.

Timeline

Start
2026-03-07
Primary completion
2028-06-06
Completion
2028-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ornidazole Other / unclassified 7 unknown Other
Subject Ornidazole Other / unclassified 100 ml Other
Background Lactulose Other / unclassified 25 ml Oral
Background Rifaximin Other / unclassified 0.4 g Oral