Last updated: February 19, 2025
Sponsor: Universitätsklinikum Hamburg-Eppendorf
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
urethal perfusion index monitoring
Clinical Study ID
NCT06799832
2024-101408-BO-ff
Ages > 45 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
at least 45 years old
scheduled for elective major abdominal surgery (involving visceral organs with anexpected duration of at least 120 minutes)
indication for an arterial catheter
indication for an urinary catheter
Exclusion
Exclusion Criteria:
Pregnancy
Planned surgery: nephrectomy, liver or kidney transplantation surgery
Patients who previously had surgery on the urethra or bladder
Patients without clinical indication for continuous blood pressure monitoring withan intraarterial catheter
Study Design
Total Participants: 116
Treatment Group(s): 1
Primary Treatment: urethal perfusion index monitoring
Phase:
Study Start date:
January 21, 2025
Estimated Completion Date:
July 31, 2025
Connect with a study center
University Medical Center Hamburg-Eppendorf
Hamburg,
GermanyActive - Recruiting
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