Evaluation of sexual function in adult patients with congenital anatomical anomalies of lower gastro-intestinal tract or pelvic region.

Completed

Conditions: anorectal malformation
Hirschsprung's disease
sacrococcygeal teratoma
colorectal birth defect
10027664
10013356

Registration Number: NL-OMON38538

Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

- Over 18 years of age at time of study, i.e. born before or in 1995.
- Anorectal malformation, Hirschsprung*s disease, or sacrococcygeal teratoma, treated in one of the participating centers.

Exclusion Criteria

- Known with mental impairment (for example retrieved from medical record that the patient suffers from a syndrome with mental retardation such as Down*s syndrome), i.e. not capable of completing the questionnaires.

Study & Design

Study Type: Observational non invasive

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters are the outcomes of the questionnaires used as<br /><br>follows. For the exact content of the questionnaires we refer to section F1.<br /><br>All the used questionnaires (including the quality of life questionnaire<br /><br>mentioned in the secondary study parameters/endpoints) are used in<br /><br>international studies, are validated in Dutch, and cross-culturally normed. For<br /><br>these questionnaires, cut-off values are available in defining what is normal<br /><br>and what is sexual dysfunction.<br /><br><br /><br>For female patients:<br /><br>- Female sexual function index (FSFI): 19 items about sexual function.<br /><br>- Female sexual distress scale (FSDS): 12 items about sexual distress.<br /><br><br /><br>For male patients:<br /><br>- International index of erectile function (IIEF): 15 items about sexual<br /><br>function and distress combined.</p><br>

Secondary Outcome Measures