CERebral Blood flow Evaluation and Regulation by UltraSound to improve neurocognitive outcome after cardiopulmonary bypass

Not Applicable

• Conditions: F05.8; U51; Other delirium

• Registration Number: DRKS00013583
• Lead Sponsor: niversitätsklinikum Bonn

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-03-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

cardiac surgery with CPB, valve surgery, coronary artery bypass

Exclusion Criteria

emergency procedures, aortic arch surgery, hypothermic perfusion <32°C

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
POD on first 3 postoperative days as assessed by the confusion assessment method (CAM) or CAM-ICU test (confusion assessment method for the intensive care unit) on the first 3 postoperative days

Secondary Outcome Measures

Name	Time	Method
postoperative cognitive deficit on 6. postoperative day as assessed by the 6-item screening test