Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00135148|
Recruitment Status : Completed
First Posted : August 25, 2005
Last Update Posted : December 28, 2007
Participants fill out a questionnaire on libido and their possible partner relationship.
A blood sample is taken for sex steroid analysis.
|Condition or disease||Intervention/treatment|
|Transsexualism||Procedure: Filling out a questionnaire on libido and possible partner relationship Procedure: Sex steroid analysis|
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.
|Study Type :||Observational|
|Enrollment :||150 participants|
|Official Title:||Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group|
|Study Start Date :||April 2004|
|Actual Study Completion Date :||August 2005|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00135148
|University Hospital Ghent|
|Ghent, Belgium, 9000|
|Principal Investigator:||Guy T'Sjoen, MD||University Hospital, Ghent|