Reducing Cardiac-surgery Associated Acute Kidney Injury Occurence by Administering Angiotensin II

Recruiting Phase 3 Interventional Study
Cardiac Surgery Vasoplegia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
1,022 (estimated)
Sponsor
Universität Münster · Other
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About This Trial
The study intervention focuses on exploring the use of angiotensin II as a primary vasopressor compared to norepinephrine in cardiac surgery patients to investigate whether angiotensin II can reduce the occurrence of moderate/severe acute kidney injury (AKI). Despite its potential, as suggested by trials involving surgical patients, there is currently no human data confirming its effectiveness in …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Cardiac surgery using cardiopulmonary bypass including coronary artery bypass grafting (CABG) surgery, valve surgery, or combined CABG/valve surgery 2. Elevated risk of AKI as predicted by a score ≥ 1.5 on the following scale: 1. hemoglobin \< 130g/l = 2 2. creatinine …
Contacts

Alexander Zarbock, MD

+49-251-8347252

PAN-AKI@ukmuenster.de

CONTACT

Melanie Meersch-Dini, MD

+49-251-8347255

PAN-AKI@ukmuenster.de

CONTACT