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Clinical Trials in Canada / NCT06802224
Recruiting Phase 4

The Choice of Vasopressor to Prevent Postoperative Acute Kidney Injury After Major Non-Cardiac Surgery

NCT06802224 · tracked via the Priya Life Science Canada tracker
Phase
Phase 4
Started
2025-04-01
Last updated
2026-05-26

Condition(s) studied

AnesthesiaSurgery With General AnesthesiaNoncardiac SurgeryHypotension During SurgeryAcute Kidney Injury (AKI)Myocardial Injury After Noncardiac Surgery (MINS)Vasopressor

Investigational drug(s) / intervention(s)

Norepinephrine →Phenylephrine →

Norepinephrine: Intravenous Norepinephrine for both infusion and bolus dosing

Phenylephrine: Intravenous Phenylephrine for both infusion and bolus dosing

Study summary

Low blood pressure, also known as hypotension, is very common during major surgery under general anesthesia. Prolonged or severe hypotension can lead to complications such as kidney injury after surgery that slow down patient recovery. Anesthesiologists commonly administer medications called vasopressors to treat low blood pressure during surgery. These medications help raise the blood pressure back up to a safe range. Two vasopressor medications are commonly used for this purpose: norepinephrine and phenylephrine. Each of these medications has slightly different effects on the heart and blood vessels (cardiovascular system). It remains unknown which of these standard medications is better for treating low blood pressure during surgery. The goal of this clinical trial is to determine which of these two medications is better at preventing injury to the kidneys after major noncardiac surgery as well as other complications such as heart problems. Major surgeries are defined as those lasting at least two hours under general anesthesia. This trial will randomize about ten centers in North America to use either norepinephrine or phenylephrine as the primary medication to treat low blood pressure in adults undergoing major noncardiac surgery. Each hospital will prioritize one of the drugs each month, and the assigned drug will rotate each month at each hospital. No further participant involvement will be required as de-identified data are collected as part of standard medical care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older * Surgery under general anesthesia with a surgery duration of 2 hours or more * Received intravenous vasopressors during surgery Exclusion Criteria: * Cardiac surgery * Extra-corporeal membrane oxygenation * Organ transplantation * Obstetric procedures * Procedures on the kidney * Outpatient procedures * Already receiving NE or PE or inotropes before induction of anesthesia (at the time of anesthesia start) * American Society of Anesthesiologists physical status classification 5 or 6 * Patient for whom a local protocol recommends a specific first line vasopressor * Most recent documented estimated glomerular filtration rate (eGFR) \< 15 mL/min/1.73m\^2 or preoperative renal replacement therapy within 60 days before surgery * Patients who do not have a preoperative creatinine value within 60 days before surgery * Alive patients who do not have a postoperative creatinine value

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
University of California, San Francisco San Francisco California Recruiting
University of Maryland College Park Maryland Recruiting
University of Michigan Ann Arbor Michigan Recruiting
Henry Ford Health Detroit Michigan Recruiting
Duke University Medical Center Durham North Carolina Recruiting
Wake Forest University School of Medicine Winston-Salem North Carolina Recruiting
UT Southwestern Medical Center Dallas Texas Recruiting
University of Virginia Charlottesville Virginia Recruiting
University of Washington Seattle Washington Recruiting
University Health Network Toronto Ontario Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06802224 on ClinicalTrials.gov ↗ ← All trials in Canada