Patient Reported Outcome After Bariatric Surgery

Recruiting now

Conditions studied: Anesthesia, Analgesia, Bariatric Surgery

In brief

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.

Key facts

Study ID

NCT03490630

Run by

Insel Gruppe AG, University Hospital Bern

People needed

2000

Starts

2011-01-02

Expected to finish

2027-12-01

Last updated by the study team

2026-01-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 years and older
• Written informed consent
• Elective bariatric surgery
• Patients' ability to understand the purpose of the study

You may not qualify if…

• No informed consent
• Cognitive impairment

Where it is running

• Department of Anaesthesiology and Pain Medicine, Inselspital, University of Bern — Bern, Switzerland (enrolling)

Full record on ClinicalTrials.gov

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