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EndogenousTestosterone Response to a Testosterone Boosting Supplement

Not Applicable
Conditions
Testosterone
Interventions
Dietary Supplement: Testosterone boosting supplement
Dietary Supplement: Placebo Comparator
Registration Number
NCT02600650
Lead Sponsor
Canadian Memorial Chiropractic College
Brief Summary

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.

Detailed Description

The experimental intervention in this study is the daily administration of a testosterone boosting supplement or sham supplement for 4 weeks. The supplement will be administered daily in capsule form. The control group will be given a sham capsule containing the carrier components of the supplement. Participants will be asked not to modify their current lifestyle. Salivary testosterone levels will be assessed prior to the intervention to collect a baseline measurement for each subject, and following the intervention to evaluate any changes in hormone levels.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Male
Target Recruitment
60
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ExperimentalTestosterone boosting supplementReceive daily authentic Testosterone boosting supplement
PlaceboPlacebo ComparatorReceive daily placebo supplementation
Primary Outcome Measures
NameTimeMethod
Change in concentration of salivary free testosterone from baseline measured by ELISA4 weeks

Change in concentration of salivary free testosterone from baseline to 4 weeks will be measured by ELISA

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Canadian Memorial Chiropractic College

🇨🇦

Toronto, Ontario, Canada

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