Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00135148

Enrollment

150

Registered

2005-08-25

Start date

2004-04-30

Completion date

2005-08-31

Last updated

2007-12-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transsexualism

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.

Interventions

PROCEDUREFilling out a questionnaire on libido and possible partner relationship

PROCEDURESex steroid analysis

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

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

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026