Postoperative DeliriumPostoperative Cognitive DysfunctionCognitive DeclineCognitive ImpairmentCognition DisordersCardiac Surgery
Investigational drug(s) / intervention(s)
CogCheck
CogCheck: Performance of study participants in the application
Study summary
This observational cohort study is designed to validate the CogCheck application as a risk prediction tool for postoperative delirium in patients undergoing cardiac surgery.
Eligibility
Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Elective cardiac surgery
* Age ≥60 years
* Good knowledge of the German language
* Written informed consent
Exclusion Criteria:
* Emergency surgery
* Medical instability limiting preoperative assessment
* Surgical procedures without the use of cardiopulmonary bypass
* Procedures involving deep hypothermic circulatory arrest
* Concurrent carotid surgical procedures
* Participation in an interventional trial with POD or POCD as primary endpoint
Primary outcome measure(s)
Postoperative delirium — Three times daily from postoperative day 1 until discharge from the intensive care unit (ICU) or intermediate care unit (IMC), assessed up to 50 days Postoperative delirium as defined by an Intensive Care Delirium Screening Checklist (ICDSC) score greater or equal to 4
Trial sites (1)
Facility
City
Region
Status
University Hospital Basel
Basel
Switzerland
Recruiting
More University Hospital, Basel, Switzerland trials in Switzerland
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.
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