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Urethral PeRfusion Index-Guided Hemodynamic ManagemenT in Patients Having Major Abdominal Surgery: the UPRIGHT Randomized Feasibility Trial
Sponsor: Universitätsklinikum Hamburg-Eppendorf
Summary
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.
Key Details
Gender
All
Age Range
45 Years - Any
Study Type
INTERVENTIONAL
Enrollment
116
Start Date
2025-01-21
Completion Date
2025-07-31
Last Updated
2025-02-21
Healthy Volunteers
No
Interventions
urethal perfusion index monitoring
The urethral perfusion index will be monitored using the IKORUS System (Vygon, Écouen, France)
Locations (2)
University Medical Center Hamburg-Eppendorf
Hamburg, Germany
University Medical Center Hamburg-Eppendorf
Hamburg, Germany