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Not yet recruiting NCT07265817

Fecal Microbiota Transplantation for Decolonization of Multidrug-resistant Microorganisms

No phase Interventional Carbapenem-Resistant Enterobacteriaceae Colonization

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Fecal Microbial transplant Capsules, Placebo.
Who it may be relevant to
Registry conditions: Carbapenem-Resistant Enterobacteriaceae Colonization. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Fecal Microbiota Transplantation for Decolonization of Multidrug-resistant Microorganisms: Randomized Double Blinded Study

Overview

The aim of the study is to see whether fecal microbiota transplantation is effective to decolonize multidrug-resistant organisms.

Interventions

  • Combination product Fecal Microbial transplant Capsules
    3 pills per day for 3 consecutive days with placebo comparatator
  • Combination product Placebo
    The same amount and shape capsules

Primary outcome measures

  • Conversion to negative organism [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Patients who have positive results in PCR or culture of rectal swab.

Exclusion criteria

  • Not provide a consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07265817 · KNUH 2023-07-013

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗