Perioperative assessment of cerebral ischemia in patients undergoing aortic arch surgery

Recruiting

• Conditions: Ischemia; stroke; 10014623; 10002363

• Registration Number: NL-OMON49005
• Lead Sponsor: IC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

- Adult patients
- Elective aortic arch surgery

Exclusion Criteria

- History of (ischemic) neurological disease, known to influence cerebral blood
flow and oxygenation
- Rescue/Emergency procedure
- Failure to obtain informed consent

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters is the dose of cerebral ischemia. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary parameters include factors that influence cerebral ischemia, such as<br /><br>cerebral autoregulation and neuronal activity, and effects of ischemia, such as<br /><br>changes in neurological and cognitive tests and delirium and biomarkers of<br /><br>ischemia. </p><br>