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Completed

NCT Number: NCT00737412

Efficacy of BIO-K+ CL1285® Prophylaxis in the Prevention of Traveler's Diarrhea in Adults

The purpose of this study is to determine the efficacy of Bio-K+ CL1285 in reducing traveler's diarrhea.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Clinique Santé Voyage des Prairies, Joliette, Quebec, Canada

Loading trial locations.

About this study

Determine efficacy of Bio-K+ CL1285 in reducing Traveler's Diarrhea by comparing the incidence of diarrhea in travelers during their stay abroad and upon their return to Canada following either Bio-K+ CL-1285 OR placebo prophylaxis.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female subjects over 18 years of age traveling to Mexico, Central America, South America and Caribbean Islands as direct destinations or on cruises to the same destinations.
  • The trips last a minimum of 7 days and a maximum of 21 days.
  • Women of child bearing capacity who are not pregnant at the moment of screening (pregnancy test done on-site) and agree to use an acceptable form of birth control for the duration of the study (e.g. Condom, oral contraceptives, etc.) are allowed to participate.

Exclusion criteria

  • active diarrhea;
  • pregnancy; breastfeeding
  • 3 diarrheic episodes within 24 hours in the 15 days preceding the date of the departure;
  • antibiotic treatment during the last 15 days or ongoing treatment at the time of departure;
  • consumption of fermented milk, yogourt or probiotics probiotics in the 15 days preceding the date of the departure;
  • immunosuppressed state or any health condition being susceptible to decompensate during the study (including malignant hemo-pathologies, AIDS, bone marrow transplant or organ transplant).
  • active radiotherapy or chemotherapy as cancer treatment
  • the administration of an ETEC/cholera vaccine or any other diarrhea vaccine in the three months prior to study initiation
  • an active, non-controlled intestinal disease;
  • ileostomy, jejunostomy or colostomy
  • concomitant participation in another clinical trial
  • mental or other conditions, or language barriers rendering the subject unable to understand the nature, scope, and possible consequences of the study or complete the self-administered questionnaires;
  • subject unlikely to comply with protocol, e.g., uncooperative attitude, and unlikelihood of completing the study,
  • allergies to any ingredients in the study product (active product or placebo)
  • current use of illicit drug and alcohol abuse

Treatment and study plan

Probiotic: Bio-K+ CL1285

Other

The probiotic Bio-K+ CL1285 RX®, a mixture of Lactobacillus acidophilus and Lactobacillus casei, contains over 50 billion living bacteria per administered dose.

Other names: Bio-K+ CL1285 RX®

Placebo

Other

Matching capsules devoid of microorganisms

Primary outcomes

  1. To determine the efficacy of Bio-K+ CL1285 RX® in reducing traveler's diarrhea by comparing the incidence of diarrhea in travelers during their stay abroad and upon their return to Canada, following either BIO-K+CL1285 RX® or placebo prophylaxis.

    Time frame: March 2008 to April 2009

Secondary outcomes

  1. To compare the severity of diarrhea in travelers during their stay abroad and upon their return to Canada, following either BIO-K+CL1285 RX® or placebo prophylaxis.

    Time frame: March 2008 to April 2009

  2. To compare the safety profile of BIO-K+CL1285 RX® to that of placebo

    Time frame: March 2008 to April 2009

  3. To compare the physician and traveler satisfaction following daily prophylaxis with either BIO-K+CL1285 RX® or placebo

    Time frame: March 08 to April 09

  4. To evaluate and compare the health economic impact of daily prophylaxis with BIO-K+CL1285 RX®.

    Time frame: March 08 to April 09

Sponsors and collaborators

Lead sponsor

Bio-K Plus International Inc.

Industry

Collaborators

  • ethica Clinical Research Inc.

Registry information

Official study title

A Double-blind, Randomized, Placebo Controlled, Multicenter Study of the Efficacy of BIO-K+ CL1285® Prophylaxis in the Prevention of Traveler's Diarrhea in Adults.

Important dates

Study start
2008
Primary completion
2009
Study completion
2010
First posted
Aug 19, 2008
Registry last updated
Jan 21, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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