Home › Aneurysms › NCT06487585
ANG-First Trial (Angiotensin II as First-Line Vasopressor Therapy in Cardiac Surgery)
RecruitingPhase 4Healthy volunteers welcome
Angiotensin II as First-Line Vasopressor Therapy in Cardiac Surgery (ANG-First Trial)
Who can join
Ages 18 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Adult patients ≥ 18 years of age undergoing cardiac surgery requiring CPB * Patients must have clinical features of vasodilation as determined by a MAP \< 65 mmHg that is non-transient in the opinion of the treating physician * Patients must be adequately volume resuscitated in the opinion of the treating physician * Systemic Vascular Resistance index (SVRi) \< 1970 dynes·sec/cm⁵/m² to support the clinical diagnosis of vasodilation; if no pulmonary artery catheter is in place, vasodilatory hypotension diagnosis according to the judgement of the critical care team * Biventricular systolic function is at or greater than pre-cardiopulmonary bypass baseline as demonstrated by echocardiographic evaluation, or the patient is concomitantly treated with Exclusion Criteria: * Bleeding as primary etiology of hypotension, as determined by \> 4 units RBC transfusion in 24 hours. * Patients on ECMO * Patients with active endocarditis * Patients already on renal replacement therapy or creatinine of \> 4 mg/dl within 2 weeks of surgery * Patients with contraindications to Angiotensin II including women who are pregnant or breastfeeding or have active coronary ischemia, mesenteric ischemia, limb ischemia, or high potassium (\> 5.5 meq/L) while receiving Angiotensin II
About the study
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.
What is being tested
- Angiotensin II (drug)
Sponsor: University of Maryland St. Joseph Medical Center · Participants: 100 · Started: May 6, 2025
Contact the study team
- Aja Janyavula · Phone: 410-427-5459
- Sam Rudow · Phone: 410-427-5459
Official record on ClinicalTrials.gov — NCT06487585
Locations in the U.S.
| Maryland | University of Maryland St. Joseph Medical Center, Towson |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.