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RECRUITING
NCT06324461
PHASE4

GLP-1 Receptor Agonist for Reduction of Myocardial Injury After Non-cardiac Surgery

Sponsor: The University of Hong Kong

View on ClinicalTrials.gov

Summary

This is an investigator initiated, multi-center, open-labelled, superiority randomized controlled trial of 372 patients undergoing elective non-cardiac surgery. Recruited patients will be randomized in a 2:1 ratio to receive single subcutaneous dose of Glucagon-like Peptide-1 Receptor Agonist (GLP-1 RAs) 1 to 14 days prior to surgery or receive routine care. Dulaglutide (Trulicity; Eli Lilly, USA) is chosen as GLP-1 Receptor Agonists investigational drug for this study. Apart from peri-operative routine care, all recruited subjects will undergo physical, respiratory and cardiac assessments including electrocardiography and blood check including cardiac enzymes. Myocardial injury, cardiovascular outcomes and safety will be assessed and evaluated for efficacy and safety of this prophylactic measurement for the reduction of myocardial injury after non-cardiac surgery.

Official title: Glucagon-like Peptide-1 Receptor Agonist for Reduction of Myocardial Injury After Non-Cardiac Surgery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

372

Start Date

2024-03-20

Completion Date

2028-12-31

Last Updated

2025-08-22

Healthy Volunteers

No

Interventions

DRUG

Dulaglutide 0.75mg subcutaneous injection

Subject randomized into treatment group will receive single subcutaneous dose of Dulaglutide 0.75mg 1 to 14 days prior to surgery

Locations (3)

Duchess of Kent Children's Hospital at Sandy Bay

Hong Kong, Hong Kong SAR, China

Queen Mary Hospital

Hong Kong, Hong Kong SAR, China

Tung Wah Hospital

Hong Kong, Hong Kong SAR, China