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
Name Time Method Pharmacokinetics 72 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
Name Time Method
Trial Locations
- Locations (1)
QPharm
š¦šŗBrisbane, Queensland, Australia