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We will perform this single-center pilot trial to determine if the intraoperative urethral perfusion index is higher in patients assigned to maintaining postinduction baseline urethral perfusion index than in patients assigned to routine care (with blinded urethral perfusion index monitoring). As pre-planned substudies, we will also assess the agreement between a) urethral perfusion index-derived pulse rate and heart rate measured with an electrocardiogram and b) between the urethral perfusion index and the peripheral perfusion index.
Age
45 - No limit years
Sex
ALL
Healthy Volunteers
No
University Medical Center Hamburg-Eppendorf
Hamburg, Germany
University Medical Center Hamburg-Eppendorf
Hamburg, Germany
Start Date
January 21, 2025
Primary Completion Date
June 30, 2025
Completion Date
July 31, 2025
Last Updated
February 21, 2025
116
ESTIMATED participants
urethal perfusion index monitoring
DEVICE
Lead Sponsor
Universitätsklinikum Hamburg-Eppendorf
NCT07043192
NCT07473869
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