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A Parallel Study Evaluating the Safety of Lactospore® in Healthy Individuals

NCT02176889 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-09-09

No results posted yet for this study

Summary

The purpose of this study is to determine whether Lactospore is safe in healthy adults.

Conditions

  • Healthy

Interventions

DIETARY_SUPPLEMENT

Lactospore

Bacillus coagulans MTCC 5856

OTHER

Placebo

Sponsors & Collaborators

  • Sabinsa Corporation

    collaborator INDUSTRY

  • KGK Science Inc.

    lead INDUSTRY

Principal Investigators

  • Dale Wilson, MD · KGK Science Inc.

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2014-08-31
Completion
2014-08-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02176889 on ClinicalTrials.gov