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A Study to Evaluate the Potential for Interpersonal Transfer of Testosterone Following Single Dose Application

Completed
Conditions
Hypogonadism
Registration Number
NCT01172366
Lead Sponsor
Acrux DDS Pty Ltd
Brief Summary

The hypotheses for this study is that there is no transfer of testosterone from male (donor) subjects to female (recipient) subjects when contact is made 2 hours post application of 2% Testosterone MD-LotionĀ® if the donor has a covered application area with a T-shirt.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pharmacokinetics72 hours total

Single dose pharmacokinetic parameters (AUC0-24, AUC0-72, Cmin, Cmax, and tmax) are to be reported for total testosterone, free testosterone and DHT.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

QPharm

šŸ‡¦šŸ‡ŗ

Brisbane, Queensland, Australia

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