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Clinical Trials in Canada / NCT05188222
Starting soon Phase 4

Preoperative Maltodextrin's Effect on Cardiac Function in Cardiac Surgery

NCT05188222 · tracked via the Priya Life Science Canada tracker
Phase
Phase 4
Started
2025-12-01
Last updated
2025-02-24

Condition(s) studied

Left Ventricular DysfunctionQuality of RecoveryRight Ventricular Dysfunction

Investigational drug(s) / intervention(s)

Maltodextrin solutionPlacebo solution

Maltodextrin solution: The oral preparation of 50 grams of Maltodextrin solution mixed in 400 mL of water

Placebo solution: Specifically formulated placebo to provide a similar taste and texture to Maltodextrin, without the same carbohydrate characteristics

Study summary

A randomized, controlled, double-blinded clinical trial evaluating the effect of the administration of a Maltodextrin solution on cardiac function in patients presenting for coronary artery bypass grafting surgery with a reduced left ventricular ejection fraction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 18 years of age or older * Presenting for coronary artery bypass grafting surgery * Preoperative left ventricular ejection fraction \< 50% * First case of the day (7:30am start time) Exclusion Criteria: * Dysphagia, gastroparesis * Cannot tolerate oral intake * Celiac disease * Type 1 diabetes

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Jewish General Hospital Montreal Quebec

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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 NCT05188222 on ClinicalTrials.gov ↗ ← All trials in Canada