The GUARDIAN Trial

Recruiting N/A Interventional Study
Blood Pressure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
45 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
6,254 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial
An international randomized trial to test the primary hypothesis that perioperative tight blood pressure management reduces a composite of major perfusion-related complications (myocardial injury, stroke, non-fatal cardiac arrest, Stage 2-3 acute kidney injury, deep or organ-space infection, sepsis, and death) in the 30 days after major non-cardiac surgery. The treatments will be: 1) norepinephri…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. At least 45 years old; 2. Scheduled for major noncardiac surgery expected to last at least 2 hours; 3. Having general anesthesia, neuraxial anesthesia, or the combination; 4. Expected to require at least overnight hospitalization (planned ICU admission is acceptable); 5. Are …
Contacts

Valerie L. Anderson, BS

(713) 500-4383

Valerie.L.Anderson@uth.tmc.edu

CONTACT

Daniel Sessler, MD

(713) 500-3062

Daniel.Sessler@uth.tmc.edu

CONTACT