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Trial registered on ANZCTR
Registration number
ACTRN12609000441213
Ethics application status
Approved
Date submitted
14/05/2009
Date registered
12/06/2009
Date last updated
12/06/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Probiotic Preparation of Bacillus coagulans: Is It a
Viable Adjunct Therapy for Relieving Symptoms of Osteoarthritis?
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Scientific title
A Randomized, Placebo-Controlled Trial of a Patented Preparation of Bacillus coagulans as Adjunct Therapy for the Relief of Symptoms in Osteoarthritis
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
mild to moderate osteoarthritis
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Condition category
Condition code
Musculoskeletal
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Osteoarthritis
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Bacillus coagulans GBI-30, 6086 is a patented strain of probiotic lactic-acid producing bacteria. It was taken in caplet form orally with water once daily for up to 60 days. Each caplet/dose contained 2 x 10 9 colony-forming units (CFUs).
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
Identically appearing placebo caplet (985 mg) containing microcrystalline cellulose was taken orally with water once daily for 60 days,
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Measures of functional capacity and symptom severity of osteoarthritis affecting the knee or back. Patients were assessed at baseline, 30 days, and 60 days from the start of treatment using the Knee Injury and Osteoarthritis Outcome Scale (KOOS) or the Oswestry Disability Questionnaire.
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Assessment method [1]
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Timepoint [1]
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60 days following the commencement of treatment.
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Secondary outcome [1]
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Safety. Adverse events such as gas, cramps, or diarrhea were reported directly to each investigator.
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Assessment method [1]
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Timepoint [1]
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60 days following the commencement of treatment.
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Eligibility
Key inclusion criteria
Adult men and women with a documented history of mild to moderate osteoarthritis for at least 12 months and had not started any new therpay within the last 3 months
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Minimum age
18
Years
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Maximum age
64
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Women of child bearing age, current probiotic usage, antibiotic therapy over the last 2 weeks, no new therapy within the last 3 months, kidney and liver disease
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/07/2005
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
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Actual
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Sample size
Target
33
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Ganeden Biotech Inc.
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Address [1]
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5915 Landerbrook Dr. Suite 304
Mayfield Heights, OH 44124
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Country [1]
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United States of America
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Primary sponsor type
Individual
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Name
Keith Lamberson, MD
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Address
Pinnacle Orthopedics & Sports Medicine Specialists
1668 Mulkey Road
Austell, GA 30106
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Country
United States of America
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Sterling Institutional Review Board (Atlanta, GA)
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Ethics committee address [1]
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Ethics committee country [1]
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Date submitted for ethics approval [1]
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Approval date [1]
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Ethics approval number [1]
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Summary
Brief summary
Certain probiotics have demonstrated the ability to lessen the symptoms of arthritis in animals and humans. This clinical trial was conducted to evaluate the effects of the probiotic Bacillus coagulan GBI-30, 6086 as adjunct therapy for the relief of symptoms of mild to moderate osteoarthritis.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Keith Lamberson, MD
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Address
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Pinnacle Orthopedics & Sports Medicine Specialists
1668 Mulkey Road
Austell, GA 30106
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Country
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United States of America
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Phone
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1-770-944-3303
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Keith Lamberson, MD
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Address
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Pinnacle Orthopedics & Sports Medicine Specialists
1668 Mulkey Road
Austell, GA 30106
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Country
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United States of America
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Phone
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1-770-944-3303
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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