Predicting Delirium Risk After Heart Surgery Using a New Cognitive Tool

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort study aims to validate the CogCheck application as a tool for predicting the risk of postoperative delirium in elderly patients undergoing cardiac surgery. The study focuses on identifying high-risk individuals by assessing cognitive performance prior to surgery, as pre-existing cognitive impairment is a significant risk factor for postoperative cognitive decline. By utilizing a self-administered tablet program, the study seeks to improve the detection of cognitive issues that are often overlooked in clinical settings. The ultimate goal is to enhance preventive strategies for delirium and cognitive dysfunction in this vulnerable population.

Why it matters

Who can join: the full rules

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

Where it's running

• University Hospital Basel
  Basel, Switzerland Recruiting

Study contacts

• Principal investigator: Nicolai Goettel, MD — University Hospital, Basel, Switzerland
• Study coordinator: Nicolai Goettel, MD
• Email: nicolai.goettel@usb.ch
• Phone: +41 61 556 5228

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Assessing brain activity patterns to predict postoperative delirium

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.