Prospective study on the treatment of congenital vaginal agenesis or vaginal hypoplasia - genital reconstruction, gynecological and urological aspects, psychosexual and social aspects and quality of life

Recruiting

• Conditions: intersex; Disorders of sex development; hermaphroditism; 10038608; 10010612; 10029903

• Registration Number: NL-OMON36303
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 545

Inclusion Criteria

Females with a disorder in sex development (DSD) and vaginal hypoplasia / aplasia
46 XY, and assigned and raised female
46, XX and assigned and raised female

Exclusion Criteria

- female DSD patients who will not start vaginal dilatation therapy
- moderate to severe mental retardation (IQ below 55)
- younger than 12 years of age

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Vaginal depth at the end of treatment<br /><br>Capability of penile-vaginal intercourse<br /><br>.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Satisfaction with sexual functioning</p><br>