Impact of Combined PSi + NIRS Monitoring in the Prevention of Postoperative Cognitive Disorders in Cardiac Surgery.
Recruiting
N/A
Interventional Study
Postoperative Cognitive Disorders
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 80 (estimated)
- Sponsor
- Brugmann University Hospital · Other
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About This Trial
Advances in cardiac medicine and anesthesia have made it possible to expand the indications for open heart surgery to increasingly older and more complex patients. This development is taking place in a demographic context where the aging of the world population has become a structural reality. However, postoperative neurocognitive complications, and in particular postoperative cognitive disorders …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Elective or relatively emergency surgery for valve surgery (pulmonary or tricuspid valves) or coronary artery bypass grafting (CABG)
* Preoperative cognitive assessment MoCA ≥ 20 (during the preoperative consultation if applicable or on day 1)
* ASA score II to IV
Exclusion C…
Contacts