Genetic Variants and Perioperative Morbidity and Mortality
Recruiting
Observational Study
Anesthesia
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.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 20,000 (estimated)
- Sponsor
- Insel Gruppe AG, University Hospital Bern · Other
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About This Trial
Prospective association study to analyse perioperative patients' outcome. Outcome comprises intraoperative and postoperative complications e.g. cardio-vascular events, allergic reactions, Possible variables which might have on influence: patient- and surgery-related data, patients' genetic background etc.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 18 years and older
* Written informed consent
* Scheduled surgery
Exclusion Criteria
* No informed consent
* Cognitive impairment
Contacts