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EndogenousTestosterone Response to a Testosterone Boosting Supplement

NCT02600650 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2015-11-09

No results posted yet for this study

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.

Conditions

  • Testosterone

Interventions

DIETARY_SUPPLEMENT

Testosterone boosting supplement

Proprietary formulation of Testosterone boosting supplement administered daily

DIETARY_SUPPLEMENT

Placebo Comparator

Daily administration of Placebo Comparator

Sponsors & Collaborators

  • Iovate Health Sciences International Inc

    collaborator INDUSTRY

  • Canadian Memorial Chiropractic College

    lead OTHER

Principal Investigators

  • brian budgell, Ph.D. · Canadian Memorial Chiropractic College

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02600650 on ClinicalTrials.gov