Randomized prospective study for comparison of patient contentment in rigid and flexible rectoscopy
Phase 4
- Conditions
- K62.9Disease of anus and rectum, unspecified
- Registration Number
- DRKS00017712
- Lead Sponsor
- Klinik für Allgemeine, Viszeral- und Transplantationschirurgie Universitätsklinik Tübingen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
Indication for diagnostic rectoscopy
Exclusion Criteria
- under age patients
- incapability to give informed consent
- oncologic entities
- status after rectal or rectosigmoid resection
- stenosis of the anal canal
- other non specified indication for rigid rectoscopy, only
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of patient contenment and subjective perception of pain by questionnaire. The Assessment is performed immediately after rectoscopy.
- Secondary Outcome Measures
Name Time Method maximum depth of penetration, time needed for rectoscopy