Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group
This study has been completed.
Sponsor:
University Hospital, Ghent
Collaborator:
Organon
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00135148
First received: August 24, 2005
Last updated: December 19, 2007
Last verified: December 2007
| Tracking Information | |||||
|---|---|---|---|---|---|
| First Received Date ICMJE | August 24, 2005 | ||||
| Last Updated Date | December 19, 2007 | ||||
| Start Date ICMJE | April 2004 | ||||
| Primary Completion Date | Not Provided | ||||
| Current Primary Outcome Measures ICMJE | Not Provided | ||||
| Original Primary Outcome Measures ICMJE | Not Provided | ||||
| Change History | Complete list of historical versions of study NCT00135148 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group | ||||
| Official Title ICMJE | Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group | ||||
| 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. |
||||
| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Not Provided | ||||
| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Not Provided | ||||
| Study Population | Not Provided | ||||
| Condition ICMJE | Transsexualism | ||||
| Intervention ICMJE |
|
||||
| Study Group/Cohort (s) | Not Provided | ||||
| Publications * | Not Provided | ||||
|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|||||
| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 150 | ||||
| Completion Date | August 2005 | ||||
| Primary Completion Date | Not Provided | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
|
||||
| Gender | Female | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Belgium | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00135148 | ||||
| Other Study ID Numbers ICMJE | 2004/341 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Not Provided | ||||
| Study Sponsor ICMJE | University Hospital, Ghent | ||||
| Collaborators ICMJE | Organon | ||||
| Investigators ICMJE |
|
||||
| Information Provided By | University Hospital, Ghent | ||||
| Verification Date | December 2007 | ||||
|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
|||||