ClinicalTrials.Veeva

Menu

Impact of Probiotic Regimen on Vancomycin Resistant Enterococcus Intestinal Carriage

U

University Hospital, Clermont-Ferrand

Status and phase

Unknown
Phase 4

Conditions

Vancomycin Resistant Enterococcus Intestinal Carriage

Treatments

Drug: Lactobacillus casei rhamnosus (strain Lcr 35 LC)

Study type

Interventional

Funder types

Other

Identifiers

NCT00437580
CHU63-0015

Details and patient eligibility

About

This study aims to reduce the duration of VRE intestinal carriage by the administration of Lactobacillus casei rhamnosus (strain Lcr 35 LC). Patients will be blindly randomized to be assigned to a 5 weeks regimen with the probiotic (10 9 lactobacillus bid) or to a 5 weeks regimen with placebo.A stool culture will be performed every week for 5 weeks (during the administration of treatment) then every two weeks until 3 consecutive negative stool culture for VRE.

Full description

This study aims to reduce the duration of VRE intestinal carriage by the administration of Lactobacillus casei rhamnosus (strain Lcr 35 LC). Patients will be blindly randomized to be assigned to a 5 weeks regimen with the probiotic (10 9 lactobacillus bid) or to a 5 weeks regimen with placebo.A stool culture will be performed every week for 5 weeks (during the administration of treatment) then every two weeks until 3 consecutive negative stool culture for VRE.

Enrollment

24 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >18;
  • Vancomycin Resistant Enterococcus intestinal carriage

Exclusion criteria

  • Neutropenia <1000 /mm3,
  • Immunosuppressive drugs,
  • Inhalation

Trial contacts and locations

1

Loading...

Central trial contact

Olivier LESENS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems