A prospective, longitudinal cohort study of persistent postsurgical opioid use among patients treated at a Swiss hospital
- Conditions
- Persistent postoperative opiate consuming
- Registration Number
- DRKS00029189
- Lead Sponsor
- Institut für Anästhesie und IntensivmedizinSpital Thurgau Frauenfeld
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 852
Inclusion Criteria
Adult patients after 1) hip arthroplasty, 2) spine surgery, 3) major visceral surgery (cholecystectomy, hemicolectomy, bariatric surgery etc.) 4) partial or complete prostatectomy, 5) caesarian delivery, or 6) major hand surgery
Exclusion Criteria
Patient not consenting
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Persistent postoperative opiate consuming 12 weeks after surgery assessed by phone call
- Secondary Outcome Measures
Name Time Method Persistent postoperative opiate consuming 6 weeks after surgery assessed by phone call <br>Persistent postoperative pain (verbal analouge scale) und pain killer intake in general after 6 and 12 weeks assessed by phone call