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

NCT00135148 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2007-12-28

No results posted yet for this study

Summary

Participants fill out a questionnaire on libido and their possible partner relationship.

A blood sample is taken for sex steroid analysis.

Conditions

  • Transsexualism

Interventions

PROCEDURE

Filling out a questionnaire on libido and possible partner relationship

PROCEDURE

Sex steroid analysis

Sponsors & Collaborators

  • Organon

    collaborator INDUSTRY
  • University Hospital, Ghent

    lead OTHER

Principal Investigators

  • Guy T'Sjoen, MD · University Hospital, Ghent

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-04-30
Completion
2005-08-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00135148 on ClinicalTrials.gov