The Bern Perioperative Biobank (BPBB)

Insel Gruppe AG, University Hospital Bern

Status: Completed

Conditions: Surgical Procedure, Operative; Anesthesia

Study type: Observational

Funder types: Other

Identifiers

NCT04767685

041/09f

Details and patient eligibility

About

The goal of the research is to define clinically relevant molecular markers for increased risk of peri-/ postoperative organo-dysfunctions, inflammation, adverse events and disease progression. To better understand the perioperative impact the investigators aim to determine perioperative levels of molecular markers over time in the available samples and clinical data of the Bern perioperative Biobank (BPBB) cohort to finally increase quality of perioperative care of patients by permitting preventive measures to be taken early in patients at risk.

Enrollment: 547 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• 18 years and older
• Written informed consent
• Non-emergency surgery

Exclusion Criteria

• Transient incapacity to consent or insufficient time (< 6h) to consider study participation
• No informed consent
• Cognitive impairment/Patients unable to consent
• Patients who retrospectively expressed their wish to be excluded

Trial design

547 participants in 1 patient group

All patients

Description:

Consenting patients undergoing non-emergency surgery with anesthesia