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Dietary Supplement

EndogenousTestosterone Response to a Testosterone Boosting Supplement

N/A
Waitlist Available
Led By brian budgell, Ph.D.
Research Sponsored by Canadian Memorial Chiropractic College
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks

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.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in concentration of salivary free testosterone from baseline measured by ELISA

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: ExperimentalExperimental Treatment1 Intervention
Receive daily authentic Testosterone boosting supplement
Group II: PlaceboPlacebo Group1 Intervention
Receive daily placebo supplementation

Find a Location

Who is running the clinical trial?

Canadian Memorial Chiropractic CollegeLead Sponsor
21 Previous Clinical Trials
2,764 Total Patients Enrolled
Iovate Health Sciences International IncIndustry Sponsor
9 Previous Clinical Trials
294 Total Patients Enrolled
brian budgell, Ph.D.Principal InvestigatorCanadian Memorial Chiropractic College
~6 spots leftby Jan 2026
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