Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00941356

Evaluation of the Efficacy of Bio-K+ Cl-1285® In the Nasal Decolonization of Methicillin Resistant Staphylococcus Aureus (MRSA) Carrier Patients

A Single Center, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Efficacy of Bio-K+ Cl-1285® In the Nasal Decolonization of Methicillin Resistant Staphylococcus Aureus (MRSA) Carrier Patients

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Bio-K Plus International Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Trial Objectives: Primary objective: * To evaluate the efficacy of Bio-K+CL1285® in patients with Methicillin-Resistant S. aureus (MRSA) nasal colonization by comparing the MRSA decolonization following either Bio-K+CL1285® or placebo treatment. Secondary objective: * To evaluate the safety profile of Bio-K+CL1285®.

Detailed description

Study Design: Double-blind, randomized (1:1 randomization), placebo-controlled, single center Canadian study. Patients will be randomly assigned to one of the two study products. A randomization schedule will be generated by the sponsor for each participating centre. This schedule will link patient identification numbers to one of the two study products allocated at random. The schedule will be prepared on a 1:1 randomization ratio. The study products will be labelled with the patient identification number. Patients have to be randomized in the order in which they qualify from the screening phase for inclusion in the study. Patients withdrawn from the study retain their patient number if already given. New patients must always be allotted a new identification number (PIN). Study Duration: The duration of patient participation in the study will be between 22 and 23 days. The overall duration of the study is expected to be approximately 10 months; with subject recruitment proposed to start in March 2009, the last follow-up visit is expected in May 2010. The actual overall study duration or subject recruitment period may vary. Number of Sites (inside and outside of Canada): One center in the province of Quebec will be involved in the study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTBio-K+ CL12852 capsules per day before breakfast
DIETARY_SUPPLEMENTPlacebo2 capsules per day before breakfast

Timeline

Start date
2010-01-01
Primary completion
2016-07-01
Completion
2016-07-01
First posted
2009-07-17
Last updated
2022-07-22

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00941356. Inclusion in this directory is not an endorsement.