Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group
Completed
- Conditions
- Transsexualism
- Registration Number
- NCT00135148
- Lead Sponsor
- University Hospital, Ghent
- Brief Summary
Participants fill out a questionnaire on libido and their possible partner relationship.
A blood sample is taken for sex steroid analysis.
- Detailed Description
Participants fill out a questionnaire on libido and their possible partner relationship on the website http://www.onderzoek-libido.be.
A blood sample is taken for sex steroid analysis. The relation will be investigated between testosterone, free testosterone, sex hormone binding globulin, estradiol, DHEA and androstenedione and scores on relational and sexual satisfaction and sexual desire.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
- Transsexual women with completed adaptation of the sex (all surgical procedures and hormonal treatments)
- The female control group must be 18-45 years
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University Hospital Ghent
🇧🇪Ghent, Belgium