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BIO-K+ CL1285 for Prevention of Recurrent Clostridium Difficile Infection

Primary Purpose

Recurrent Clostridium Difficile Infection

Status
Suspended
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Lactobacillus acidophilus CL1285® and Lactobacillus casei
Placebo
Sponsored by
Bio-K Plus International Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Recurrent Clostridium Difficile Infection focused on measuring Clostridium difficile, diarrhea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18 years or older
  2. Presence of two or more loose or liquid stools in the 24-hour period prior to initiation of antibiotic therapy
  3. Hospitalized and starting antibiotic therapy for Clostridium difficile infection (CDI) or recurrent Clostridium difficile infection (RCDI), diagnosed with a positive stool culture
  4. Agree to use contraception throughout study period, unless postmenopausal or surgically sterile (females only)
  5. Understand the nature and purpose of the study including potential risks and side effects
  6. Willing to comply with the requirements of the study

Exclusion Criteria:

  1. History of 2 or more clostridium difficile infections at any time prior to the current episode
  2. Presence of severe chronic and/or inflammatory condition
  3. Impaired immunity, e.g. undergoing immunotherapy or chemotherapy
  4. Major gastrointestinal complication, e.g. Crohn's disease or ulcer
  5. Current treatment with nasogastric tube, ostomy, or parenteral nutrition
  6. Use of proton pump inhibitors
  7. Pregnant female or breastfeeding
  8. Eating disorder
  9. History of alcohol, drug, or medication abuse
  10. Daily consumption of probiotics, fermented milk, and/or yogurt
  11. Known allergies to any substance in the study product
  12. Participation in another study with any investigational product within 3 months of screening

Sites / Locations

  • Parker Jewish Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotic

Placebo

Arm Description

BIO-K+ CL1285

Placebo

Outcomes

Primary Outcome Measures

Incidence of recurrent Clostridium difficile infection

Secondary Outcome Measures

Duration of recurrent diarrhea episodes
Presence of gastrointestinal symptoms
Adverse events

Full Information

First Posted
September 14, 2010
Last Updated
January 14, 2016
Sponsor
Bio-K Plus International Inc.
Collaborators
Sprim Advanced Life Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT01202630
Brief Title
BIO-K+ CL1285 for Prevention of Recurrent Clostridium Difficile Infection
Official Title
A Triple-blind, Randomized, Placebo-controlled, Multi-center Study on the Effect of BIO-K+ CL1285 for Prevention of Recurrent Clostridium Difficile Infection
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Suspended
Why Stopped
The site is unable to recruit patients.
Study Start Date
June 2010 (undefined)
Primary Completion Date
January 2016 (Anticipated)
Study Completion Date
January 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bio-K Plus International Inc.
Collaborators
Sprim Advanced Life Sciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of this study is to evaluate the efficacy of BIO-K+ CL1285 for prevention of recurrent Clostridium difficile infection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Clostridium Difficile Infection
Keywords
Clostridium difficile, diarrhea

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Probiotic
Arm Type
Experimental
Arm Description
BIO-K+ CL1285
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus acidophilus CL1285® and Lactobacillus casei
Other Intervention Name(s)
BIO-K+ CL 1285
Intervention Description
2 capsules of Lactobacillus acidophilus CL1285® and Lactobacillus casei (50 billion cfu/capsule), consumed once daily for 60 days
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
2 capsules of placebo (no live cells), consumed once daily for 60 days
Primary Outcome Measure Information:
Title
Incidence of recurrent Clostridium difficile infection
Time Frame
60 days
Secondary Outcome Measure Information:
Title
Duration of recurrent diarrhea episodes
Time Frame
60 days
Title
Presence of gastrointestinal symptoms
Time Frame
60 days
Title
Adverse events
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Presence of two or more loose or liquid stools in the 24-hour period prior to initiation of antibiotic therapy Hospitalized and starting antibiotic therapy for Clostridium difficile infection (CDI) or recurrent Clostridium difficile infection (RCDI), diagnosed with a positive stool culture Agree to use contraception throughout study period, unless postmenopausal or surgically sterile (females only) Understand the nature and purpose of the study including potential risks and side effects Willing to comply with the requirements of the study Exclusion Criteria: History of 2 or more clostridium difficile infections at any time prior to the current episode Presence of severe chronic and/or inflammatory condition Impaired immunity, e.g. undergoing immunotherapy or chemotherapy Major gastrointestinal complication, e.g. Crohn's disease or ulcer Current treatment with nasogastric tube, ostomy, or parenteral nutrition Use of proton pump inhibitors Pregnant female or breastfeeding Eating disorder History of alcohol, drug, or medication abuse Daily consumption of probiotics, fermented milk, and/or yogurt Known allergies to any substance in the study product Participation in another study with any investigational product within 3 months of screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cornelius J Foley, MD
Organizational Affiliation
Parker Jewish for Health Care and Rehabilitation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parker Jewish Institute
City
New Hyde Park
State/Province
New York
ZIP/Postal Code
11040
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20145608
Citation
Gao XW, Mubasher M, Fang CY, Reifer C, Miller LE. Dose-response efficacy of a proprietary probiotic formula of Lactobacillus acidophilus CL1285 and Lactobacillus casei LBC80R for antibiotic-associated diarrhea and Clostridium difficile-associated diarrhea prophylaxis in adult patients. Am J Gastroenterol. 2010 Jul;105(7):1636-41. doi: 10.1038/ajg.2010.11. Epub 2010 Feb 9.
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BIO-K+ CL1285 for Prevention of Recurrent Clostridium Difficile Infection

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