Ireland
--:--IST
Active, not recruiting Observational

The Inselspital Surgical Cohort Study

NCT04096885 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2019-09-09
Last updated
2026-05-05

Condition(s) studied

Surgical Site Infection

Investigational drug(s) / intervention(s)

Blood and urine samples, skin and stool swabs

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

Sex
ALL
Min age
16 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients undergoing surgery at the Department of Visceral Surgery and Medicine, Inselspital, University Hospital Bern * Who gave General consent * Study-specific written informed consent Exclusion Criteria: * None

Primary outcome measure(s)

  • Incidence of surgical site infection — 30 days
    Number of patients with surgical site infections 30 days postoperatively

Trial sites (1)

FacilityCityRegionStatus
Beldi Guido Bern Switzerland
Official registry record

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