Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group
1 other identifier
observational
150
1 country
1
Brief Summary
Participants fill out a questionnaire on libido and their possible partner relationship. A blood sample is taken for sex steroid analysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2004
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2004
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2005
CompletedFirst Submitted
Initial submission to the registry
August 24, 2005
CompletedFirst Posted
Study publicly available on registry
August 25, 2005
CompletedDecember 28, 2007
December 1, 2007
August 24, 2005
December 19, 2007
Conditions
Interventions
Eligibility Criteria
You may qualify if:
- Transsexual women with completed adaptation of the sex (all surgical procedures and hormonal treatments)
- The female control group must be 18-45 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Ghentlead
- Organoncollaborator
Study Sites (1)
University Hospital Ghent
Ghent, 9000, Belgium
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Guy T'Sjoen, MD
University Hospital, Ghent
Study Design
- Study Type
- observational
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
August 24, 2005
First Posted
August 25, 2005
Study Start
April 1, 2004
Study Completion
August 1, 2005
Last Updated
December 28, 2007
Record last verified: 2007-12