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NCT04652375

Outcomes After Albumin Vs Lactated Ringer's Solution in CABG and AVR Procedures

Completed NA Last updated 23 September 2024
What this trial tests

NA trial testing Albumin Solution in Coronary Artery Bypass Graft Surgery in 131 participants. Completed in 26 July 2022.

Timeline
1 July 2021
Primary endpoint
26 July 2022
26 July 2022

Quick facts

Lead sponsorYale University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeprevention
Enrollment131
Start date1 July 2021
Primary completion26 July 2022
Estimated completion26 July 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

18 and older, any sex, with Coronary Artery Bypass Graft Surgery or Aortic Valve Replacement. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, randomized, double-blinded study to compare the use of albumin versus lactated Ringer's solution in patients undergoing coronary artery bypass graft surgery and in patients undergoing aortic valve replacement surgery and evaluate the incidence of acute kidney injury as a primary outcome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Coronary Artery Bypass Graft Surgery

Currently open trials in the same condition.

Other Yale University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04652375.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing