Prospective observational study to analyse patients' pain related outcome after surgery and ist association to genetic variants and non-genetic variables.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* 18 years and older
* Written informed consent
* Elective surgery
* Patients' ability to understand the purpose of the study
Exclusion Criteria
* No informed consent
* Cognitive impairment
Primary outcome measure(s)
Pain related impairment after surgery and its association to genetic and non-genetic variables — day of surgery up to 1 year after surgery Measured by the International Pain Outcomes Questionnaire, the Brief Pain Inventory (BPI): Numeric rating scale for pain intensities, affective and physical interference; Composite score = pain interference total scores (PITS scale 0-10) resulting in no interference (PITS=0), mild interference (PITS \>0 and \<2), moderate interference (PITS 2-5) and severe interference (PITS \>5)
Trial sites (1)
Facility
City
Region
Status
Department of Anaesthesiology and Pain Medicine, Inselspital, University of Bern
Bern
Switzerland
Recruiting
More Insel Gruppe AG, University Hospital Bern trials in Switzerland
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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