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Patient Reported Outcome After Bariatric Surgery

NCT03490630 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2026-01-07

No results posted yet for this study

Summary

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

  • Anesthesia
  • Analgesia
  • Bariatric Surgery

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Ulrike M Stamer, Prof. MD · Department of Anaestheisology and Pain Medicine, Inselspital, University of Bern

  • Frank Stüber · Department of Anaesthesiology and Pain Medicine, Inselspital, University of Bern

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-01-02
Primary Completion
2026-12-31
Completion
2027-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03490630 on ClinicalTrials.gov