Ireland
--:--IST
Recruiting Phase 1/2

FMT to Eradicate Intestinal Colonization by Carbapenem-resistant Enterobacteriaceae

NCT05791396 · tracked via the Priya Life Science Italy tracker
Phase
Phase 1/2
Started
2024-02-08
Last updated
2025-03-12

Condition(s) studied

Enterobacteriaceae InfectionsMulti-antibiotic Resistance

Investigational drug(s) / intervention(s)

Donor - FMT →Placebo FMT

Donor - FMT: this intervention is represented by the administration, in the recipients' gut, of donor microbiota through FMT

Placebo FMT: This intervention is represented by the administration, in the recipients' gut, of a placebo through colonoscopy

Study summary

Antibiotic resistance (AR) is a critical public health threat and one of the greatest challenges of the 21st century. In an estimate of 2019, nearly 700.000 infections and 33.000 attributable deaths from multi-drug-resistant bacteria (MDRB) have occurred in Europe in 2015. The gastrointestinal tract is a large reservoir for MDRB, and the gut microbiota can harbor a collection of AR genes, called gut resistome. Preliminary nonrandomized evidence suggests that fecal microbiota transplant (FMT) could be a promising treatment option to eradicate MDRB, but established evidence, as well as mechanisms that underpin this therapeutic pathway, are still unavailable. Leveraging our expertise in FMT (OU1), microbiome (OU2) and MDRB (OU3), we aim to evaluate the efficacy of FMT (from donors with limited presence of AR genes) in eradicating intestinal MDRB through a randomized controlled trial and identifying microbial features that are associated with clinical efficacy and clearance of AR genes

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * \>18 years; * CRE diagnosed with rectal swab \<15 days before evaluation; * Ability to undergo study procedures and to give informed consent. Exclusion Criteria: * Active chronic gastrointestinal disorders; * Previous colorectal surgery; * Major comorbidities; * Pregnancy/breastfeeding; * Psychiatric disorders.

Primary outcome measure(s)

  • CRE eradication at week 4 after the end of treatments — 4 weeks
    The investigators will evaluate the number of participants who will obtain eradication of CRE carriage after treatments, at 4 weeks-follow-up, evaluated through rectal swab for CRE

Trial sites (1)

FacilityCityRegionStatus
Giovanni Cammarota Roma Italy Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05791396 on ClinicalTrials.gov ↗ ← All trials in Italy