The purpose of this research is to evaluate the use of Angiotensin II in patients with low blood pressure post-surgery. Your information will be collected for 28 days post the procedure and initiation of the study drug to assess for safety events and complications.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Angiotensin II: Starting dose of 2.5 ng/kg/min administered IV; may dose escalate up to 80 ng/kg/min in order to achieve a MAP of 65 mmHg or higher in the first 3 hours. After 3 hours, may escalate dose up to 40 ng/kg/min in order to achieve a MAP of 65 mmHg. Dose titration in increments of 10 ng/kg/min every 2 minutes.
University of Maryland St. Joseph Medical Center
Towson, Maryland, United States
RECRUITINGIncidence of postoperative acute kidney injury, atrial fibrillation
The primary endpoint will be measured by comparing the incidence of new-onset atrial fibrillation or acute kidney injury
Time frame: 28 days
Hours on Vasopressors
Time frame: 28 days
Total IVF
Time frame: 28 days
ICU LOS
Time frame: 28 days
Postoperative LOS
Time frame: 28 days
Any major STS complication
Time frame: 28 days
30-day mortality
Time frame: 30 days
Cost
Time frame: 28 days
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