Penoid construction in gender dysphoria female-to-male (trans men)
Recruiting
- Conditions
- F64.0Transsexualism
- Registration Number
- DRKS00031796
- Lead Sponsor
- rologische Klinik München Planegg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Patients with female-to-male gender dysphoria (trans male) with medical indication for penoid reconstruction.
Exclusion Criteria
Underage
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determination of the data obtained with the applied surgical technique on the target variables (see below) to enable optimal individual counseling and indication; penoid dimensions (especially in relation to forearm tissue), number of operations and complications, treatment duration, and patient satisfaction play the most important role. Data are collected during the surgeries as well as at discharge from inpatient treatment and at the outpatient follow-up visit (most recently two years after the last surgery). Data collection is performed anamnestically and by means of measurement (caliper, tape measure, protractor). Standardized and validated questionnaires are used to record quality of life and satisfaction. The questionnaires are distributed prior to each intervention and two years after the last intervention.
- Secondary Outcome Measures
Name Time Method Statement on bacterial colonization of reconstructed urethras (within routine medical follow-up). Presentation of typical examples of surgical care of complications in case studies (dissertation).