Genetic Variants and Postoperative Pain

Recruiting Observational Study
Postoperative Pain Analgesia Surgical Procedure, Operative
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
5,000 (estimated)
Sponsor
Insel Gruppe AG, University Hospital Bern · Other
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About This Trial

Prospective observational study to analyse patients' pain related outcome after surgery and ist association to genetic variants and non-genetic variables.

Trial Locations
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Eligibility Criteria
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
Contacts

Ulrike M Stamer, Prof. MD

0041-316329995

ulrike.stamer@dbmr.unibe.ch

CONTACT

Frank Stüber, Prof. MD

0041-316322483

frank.stueber@insel.ch

CONTACT