The Inselspital Surgical Cohort Study
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood and urine samples, skin and stool swabs: Blood samples will be collected before surgery, on the first postoperative day and after 3-8 weeks. Urine samples will be collected after surgery and after 3-8 weeks. Stool and skin swabs will be collected before surgery.
Study summary
Personalizing surgical care is of enormous clinical relevance, when considering the number of patients undergoing surgery in Switzerland every year. Currently, personalization is based on underlying or coexisting disease or alterations of laboratory values, but there is no accepted biological test available that may predict success or failure of surgery. Surgical site infections are the most common form of hospital-acquired infections. While the relevance of bacteria, antibiotics and intensive care support is well accepted, the impact of the individual host response remains poorly understood. The Investigators hypothesize that postoperative alterations of the metabolome allow identification of predictors of surgical complications in general, and surgical site infections in particular.
Eligibility
Primary outcome measure(s)
- Incidence of surgical site infection — 30 days
Number of patients with surgical site infections 30 days postoperatively
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beldi Guido | Bern | Switzerland |
More Insel Gruppe AG, University Hospital Bern trials in Switzerland
Other trials for the same condition
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.
View NCT04096885 on ClinicalTrials.gov ↗ ← All trials in Switzerland