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Impact of Probiotic Regimen on Vancomycin Resistant Enterococcus Intestinal Carriage

Impact of Probiotic Regimen on Vancomycin Resistant Enterococcus (VRE) Intestinal Carriage : a Double Blind Randomized Pilot Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00437580
Enrollment
24
Registered
2007-02-21
Start date
2007-02-28
Completion date
2009-08-31
Last updated
2011-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vancomycin Resistant Enterococcus Intestinal Carriage

Keywords

Vancomycin Resistant Enterococcus, probiotic

Brief summary

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.

Detailed 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.

Interventions

DRUGLactobacillus casei rhamnosus (strain Lcr 35 LC)

Patients will be blindly randomized to be assigned to a 5 weeks regimen with the probiotic or to a 5 weeks regimen with placebo.

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \>18; * Vancomycin Resistant Enterococcus intestinal carriage

Exclusion criteria

* Neutropenia \<1000 /mm3, * Immunosuppressive drugs, * Inhalation

Design outcomes

Primary

MeasureTime frame
Reduction of the duration of Vancomycin Resistant Enterococcus intestinal carriage.

Countries

France

Contacts

Primary ContactOlivier LESENS
olesens@chu-clermontferrand.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026