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Study identifier: NCT06001333 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of FMT for the Decolonization of MDROs in the Intestinal Tract

Condition: Carbapenem-Resistant Enterobacteriaceae · Vancomycin (Glycopeptide) Resistant Enterococcus (VRE)  ·  Sponsor: Chuncheon Sacred Heart Hospital

PhaseNA
Planned participants240
Who can joinAll sexes, 20 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this unblinded randomized controlled trial is to evaluate the efficacy and safety of fecal microbiota transplantation for the decolonization of carbapenemase-producing carbapenem-resistant Enterobacteriaceae (CP-CRE) or vancomycin-resistant Enterococci (VRE) in the intestinal tract. The study is planned to be conducted to test the superiority hypothesis that the decolonization success rate in the FMT group is higher compared to the non-FMT group. Outcome analysis will be conducted through intention-to-treat analysis, modified intention-to-treat analysis, and per-protocol analysis. The main questions it aims to answer are: * primary endpoint: Rate of Decolonization of Multidrug-Resistant Organisms (CP-CRE or VRE) at 1 Month After Fecal Microbiota Transplantation (FMT). * secondary endpoint: Rates of Multidrug-Resistant Organism decolonization at 3 months, 6 months, and 1 year after FMT / Post-FMT Multidrug-Resistant Organism Recolonization Rate and Infection Rate. Patients colonized with multidrug-resistant organisms in the gastrointestinal tract are divided into two groups through obtaining written consent from the patients and random allocation: the Fecal Microbiota Transplantation group (FMT group), which receives FMT, and the control group (non-FMT group), which is observed without FMT. The decolonization status of multidrug-resistant organisms will be monitored every 3-7 days after FMT until three consecutive negative results.

This description comes directly from the study's public registry record.

Talk to the study team

Seung Soon Lee, MD, PhD  ·  +82-10-3379-9347  ·  hushh93@gmail.com

Jun Yong Choi, MD, PhD  ·  +82-10-4073-9253  ·  seran@yuhs.ac

Always discuss trial participation with your own doctor first.

Locations (2)

Chuncheon Sacred Heart HospitalChuncheon, Gangwon-do, South KoreaRecruiting
Severance HospitalSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT06001333