Actively Recruiting
Patient Reported Outcome After Bariatric Surgery
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2026-01-07
2000
Participants Needed
1
Research Sites
882 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Prospective association study to analyse patients' outcome after bariatric surgery. Outcome comprises postoperative pain, analgesia, postoperative side-effects, long-lasting pain, patients' impairment in daily living.
CONDITIONS
Official Title
Patient Reported Outcome After Bariatric Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years and older
- Written informed consent
- Elective bariatric surgery
- Ability to understand the purpose of the study
You will not qualify if you...
- No informed consent
- Cognitive impairment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Anaesthesiology and Pain Medicine, Inselspital, University of Bern
Bern, Switzerland, 3010
Actively Recruiting
Research Team
U
Ulrike M Stamer, Prof. MD
CONTACT
F
Frank Stüber, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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