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Dietary Supplement
Experimental for Testosterone
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
Awards & highlights
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 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in concentration of salivary free testosterone from baseline measured by ELISA
Side effects data
From 2012 Phase 4 trial • 22 Patients • NCT0120803819%
Skin irritation
10%
Increased facial hair
5%
per vagina spotting
5%
Acne
5%
Blepharitis
100%
80%
60%
40%
20%
0%
Study treatment Arm
Testosterone
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
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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
5 Previous Clinical Trials
139 Total Patients Enrolled
brian budgell, Ph.D.Principal InvestigatorCanadian Memorial Chiropractic College
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