Testosterone Clinical Trial
Official title:
EndogenousTestosterone Response to a Testosterone Boosting Supplement
The purpose of this study is to determine whether a proprietary 'testosterone-boosting' supplement, when used as recommended by the manufacturer, results in an increase in testosterone levels as measured by a salivary free testosterone assay.
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | June 2016 |
Est. primary completion date | June 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 20 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Adult male aged 20 to 40 years. - Fluent in English. Exclusion Criteria: - Currently receiving hormonal therapy or testosterone boosting supplement. - Has received hormonal therapy or testosterone boosting supplement within 3 months prior to study. - Has experienced adverse event following previous exposure to testosterone boosting supplements. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)
Country | Name | City | State |
---|---|---|---|
Canada | Canadian Memorial Chiropractic College | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Canadian Memorial Chiropractic College | Iovate Health Sciences International Inc |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in concentration of salivary free testosterone from baseline measured by ELISA | Change in concentration of salivary free testosterone from baseline to 4 weeks will be measured by ELISA | 4 weeks | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
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