Sexual function after 'close rectal' ileo-anal pouch.
Recruiting
- Conditions
- lcerative colitisRestorative proctocolectomyIleo pouch anal anastomosisSexual functionColitis UlcerosaProctocolectomieIleo anale pouchSeksueel functioneren
- Registration Number
- NL-OMON29187
- Lead Sponsor
- Academic Medical CenterDepartment of Surgery
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 18
Inclusion Criteria
1. Female patients;
2. >17 years and pre menopausal;
Exclusion Criteria
1. Previous bowel resections other than emergency colectomy;
2. Previous surgery on genitalia;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary study endpoints are the difference in VPA pre- and postoperatively for the close rectal group and the difference in VPA pre- and postoperatively for the close rectal and the TME groups compared.
- Secondary Outcome Measures
Name Time Method Secondary endpoints are differences in feelings of sexual arousal and estimated lubrication pre- and postoperatively and difference in psychological- and sexual functioning pre- and postoperatively for the close rectal group and for the close rectal and the TME groups compared. These outcomes will be measured by means of the Subjective Self-Assessment Questionnaire (SSAQ), Female Sexual Function Index (FSFI), Female Sexual Distress Scale (FSDS), Short Form-36 (SF-36), Beck Depression Inventory (BDI) and Maudsley Marital Questionnaire (MMQ). Our other study parameters will include age, American Society of Anesthesiologists (ASA) classification, Body Mass Index (BMI), operating time, type of surgery (i.e. IPAA or IPAA with protecting loop ileostomy).