Current partner codePEPTIDESDE
NCT06324461·Phase 4·INTERVENTIONAL

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

Status

Recruiting

Phase

Phase 4

Enrollment

372

Locations

3

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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.

Full detailed description

Myocardial injury following non-cardiac surgery (MINS) is increasingly recognized as a major cause of peri-operative morbidity and mortality worldwide. MINS is defined as post-operative cardiomyocyte injury that can be detected by high-sensitive troponin assays, which may or may not be associated with symptoms or changes on electrocardiogram (ECG). Globally, it was found that 35.5% patients had MINS with elevated troponin level in the early post-operative period. Post-operative troponin T level strongly correlated with peri-operative mortality. It was demonstrated that elevated troponin T level to 14-20 ng/L after surgery significantly increased 30-day mortality with hazard ratio of 9.11. As the global volume of non-cardiac surgeries continues to increase, there is an urgent need to identify effective strategies to minimize MINS. To date, no pharmacological intervention has been shown to safely reduce MINS. This study will evaluate the effect of pre-operative glucagon-like peptide 1 receptor agonists (GLP-1 RAs) on MINS. GLP-1 is a peptide hormone produced by intestinal epithelial endocrine L-cells that stimulates insulin secretion and inhibits glucagon secretion. GLP-1 RAs have been used to treat both diabetic and non-diabetic conditions. In landmark cardiovascular outcome trials, GLP-1 RAs were shown to reduce major adverse cardiovascular events (MACE) when compared with placebo. GLP-A RAs exert beneficial effects by stabilizing atherosclerotic plaques. Animal studies revealed that a GLP-1 RAs attenuate activation and recruitment of monocytes and macrophages to the arterial wall by suppressing expression of interleukin 6 (IL-6), chemokine (C-C motif) ligand 2 (CCL2), vascular cell adhesion molecule 1 (VCAM-1), and E- selectin (SELE). GLP-1 RAs also suppress vascular smooth muscle cell proliferation and migration via the Cyclic adenosine monophosphate (cAMP) or protein kinase A (PKA) pathway. Another key advantage of using GLP-1 RA in the context of surgery is intra-operative stabilization of glycemic level. It is well established that intra-operative hyperglycemia is associated with increased risk of MINS. Prospective studies have revealed that GLP-1 RA infusion during the peri-operative period resulted in better glycemic control among diabetic and non-diabetic patients without significantly increasing hypoglycemia risk. The "Glucagon-like Peptide-1 Receptor Agonist for Reduction of Myocardial Injury after Non-Cardiac Surgery" (GLUMINS) trial is an investigator initiated, multi-center, open-labelled Randomized Controlled Trial that will determine the effect of pre-operative GLP-1 RAs on MINS. The study hypothesis is that pre-operative GLP-1 RAs will reduce myocardial injury in patients undergoing non-cardiac surgery. Critically needed new knowledge will be generated about the effectiveness of GLP-1 RAs as a peri-operative intervention to reduce MINS, which may fundamentally alter peri-operative management in non-cardiac surgeries.

Interventions

Treatment arms and agents.

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

Timeline

From registration to results.

  1. First posted

    Mar 22, 2024

  2. Study start

    Mar 20, 2024

  3. Primary completion

    Dec 31, 2028

  4. Study completion

    Dec 31, 2028

  5. Results posted

    Not reported

  6. Registry updated

    May 4, 2026

Outcomes

What the study measures.

Primary outcomes

Proportion of patients with MINS

Time frame · Within 72 hours after surgery

Defined as any elevation in troponin T \>= 14ng/L

Secondary outcomes

Proportion of patients with composite of non-fatal MINS, non-fatal stroke or cardiovascular mortality

Time frame · Within 30 days of randomization

Proportion of patients with MINS who do not fulfill the 4th universal definition of myocardial infarction

Time frame · Within 30 days of randomization

Proportion of patients with myocardial infarction according to the 4th universal definition of myocardial infarction

Time frame · Within 30 days of randomization

Proportion of patients with ischemic stroke

Time frame · Within 30 days of randomization

Proportion of patients with cardiovascular death

Time frame · Within 30 days of randomization

Proportion of patients with all-cause mortality

Time frame · Within 30 days of randomization

Mean days alive and out of hospital

Time frame · Within 30 days of randomization

Clinically important atrial fibrillation

Time frame · Within 30 days of randomization

Clinically significant hypoglycaemia

Time frame · Within 30 days of randomization

Mean peak troponin T concentration

Time frame · During the period of index hospitalization up to 3 days

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Age ≥ 18 years * Planned elective intermediate to high risk non-cardiac surgery * Anticipated to remain hospitalized for at least one night after surgery * Voluntarily agrees to participate by providing written informed consent Exclusion Criteria: * History of symptomatic hypoglycemia within 1 month of recruitment * History of pancreatitis * Diabetic retinopathy * Personal or family history of medullary thyroid carcinoma (MTC) * Multiple Endocrine Neoplasia syndrome type 2 (MEN 2) * Acute coronary syndrome, decompensated heart failure, cardiogenic shock, or myocarditis within 1 month of recruitment * Stroke or transient ischemic attack within 1 month of recruitment * Known severe liver disease (Child-Pugh B or C) * Stage 5 chronic kidney disease (estimated glomerular filtration rate (eGFR) by Modified Diet in Renal Disease (MDRD) equation \< 15 mL/min) * Recent use of GLP-1 RA within 1 month of recruitment * Known allergy or hypersensitivity to GLP-1 RA * Women of childbearing age who are not taking effective contraception, or who are pregnant or breast-feeding * Use of Dipeptidyl peptidase-4 inhibitor(DPP4i)

Study locations

3 registered sites.

China. Showing up to 24 locations stored in the fast local snapshot.

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

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Dulaglutide.

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Put the record in context.

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