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Study identifier: NCT06799832 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Urethral PeRfusion Index-Guided Hemodynamic ManagemenT in Patients Having Major Abdominal Surgery: the UPRIGHT Randomized Feasibility Trial

Condition: Urethral Perfusion Index · Tissue Perfusion · Microcirculation  ·  Sponsor: Universitätsklinikum Hamburg-Eppendorf

PhaseNA
Planned participants116
Who can joinAll sexes, 45 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Bernd Saugel, MD  ·  +49741052415  ·  b.saugel@uke.de

Moritz Flick, MD  ·  +49741052415  ·  m.flick@uke.de

Always discuss trial participation with your own doctor first.

Locations (2)

University Medical Center Hamburg-EppendorfHamburg, GermanyNot Yet Recruiting
University Medical Center Hamburg-EppendorfHamburg, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT06799832