Measurement of the patient-side quality after colorectal surgical interventions (MErkE). Clinical study for evaluation of the patient-side quality with reference to fecal and urine incontinence and sexual dysfunction after deep colorectal surgery, as compared to pre- and postoperative.
Recruiting
- Conditions
- C20Malignant neoplasm of rectum
- Registration Number
- DRKS00025156
- Lead Sponsor
- Siloah St. Trudpert Klinikum, Klinik für Allgemein-, Viszeral-, Thorax- und minimal-invasive Chirurgie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Planned surgery of a rectal adenocarcinoma (ICD-C20) and/ or rectosigmoidal. (ICD-C19)
- adequate knowledge of the language
- age over 18
- a good physical and mental constitution to allow being part of the study
- written consent of the patient
Exclusion Criteria
- age under 18
- suffering from dementia or being curated
- missing a written consent
- occurred surgical interventions of the rectum and the rectosigmoidal passage for example rectopexy
- occurred conventional or laparoscopic prostatectomy
- occurred radiotherapy of the small basin, except current neoadjuvant therapy
- anal cancer, high grade intraepithelial neoplasia or squamous cell cancer
- status post gynecological surgery, for example ovarian cancer
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Number of fecal incontinence<br>- number of urinary incontinence<br>- number of sexual dysfunction (respectively before and after surgery or else with oder without radiotherapy);<br>by means of questionnaires
- Secondary Outcome Measures
Name Time Method Influence on livability of the following factors: <br>- radiotherapy yes/ no<br>- chemotherapy yes/ no<br>- age, sex<br>- working/ unfit for work/ job-seeking or retired<br>- being in a support group<br>- postoperative complications