Effectivity of a standardized, protocol-based, postoperative visit to verify the effectiveness of a clinic-wide used postoperative acute pain standard.
- Conditions
- postoperative acute painR52R52.0Pain, not elsewhere classifiedAcute pain
- Registration Number
- DRKS00025895
- Lead Sponsor
- niversitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, Schmerztherapie Klinikum Herford AöR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 2779
Inclusion Criteria
postoperative, inpatient patients
Exclusion Criteria
none
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method