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NCT05834257

Crystalloid Fluids and Cardiac Surgery

Withdrawn NA Last updated 21 February 2025
What this trial tests

NA trial testing Normal Saline for fluid resuscitation in Surgery-Complications. Withdrawn.

Timeline
31 March 2023
Primary endpoint
19 February 2025
19 February 2025

Quick facts

Lead sponsorCentre hospitalier de l'Université de Montréal (CHUM)
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Start date31 March 2023
Primary completion19 February 2025
Estimated completion19 February 2025
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Who can join

Adults 65 to 85, any sex, with Surgery-Complications. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

All cardiac patients admitted to the intensive care unit after surgery received crystalloid fluids as standard care procedure. 3 crystalloid fluids can be used during their stay: Normal Saline, PlasmaLyte or Ringer's Lactate. They differ in their respective composition, mainly in chloride and sodium concentrations. Inflammatory consequences of the crystalloid fluids used in this population are unknown. The investigators plan to evaluate which one of the three fluids mentioned above is advantageous in cardiac surgery patients with regards to reduced rate of infection and renal failure.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Surgery-Complications

Currently open trials in the same condition.

Other Centre hospitalier de l'Université de Montréal (CHUM) 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/NCT05834257.

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