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NCT Number: NCT06324461

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

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Duchess of Kent Children's Hospital at Sandy Bay, Hong Kong, Hong Kong SAR, China

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Dulaglutide 0.75mg subcutaneous injection

Drug

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

Other names: Trulicity 0.75mg subcutaneous injection

Primary outcomes

  1. Proportion of patients with MINS

    Time frame: Within 72 hours after surgery

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

Secondary outcomes

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

    Time frame: Within 30 days of randomization

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

    Time frame: Within 30 days of randomization

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

    Time frame: Within 30 days of randomization

  4. Proportion of patients with ischemic stroke

    Time frame: Within 30 days of randomization

  5. Proportion of patients with cardiovascular death

    Time frame: Within 30 days of randomization

  6. Proportion of patients with all-cause mortality

    Time frame: Within 30 days of randomization

  7. Mean days alive and out of hospital

    Time frame: Within 30 days of randomization

  8. Clinically important atrial fibrillation

    Time frame: Within 30 days of randomization

  9. Clinically significant hypoglycaemia

    Time frame: Within 30 days of randomization

  10. Mean peak troponin T concentration

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

  11. Mean area under curve of troponin T concentration

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

Other outcomes

  1. Proportion of patients with coronary revascularization

    Time frame: Within 30 days of randomization

  2. Proportion of patients who require readmission for cardiovascular conditions

    Time frame: Within 30 days of randomization

  3. Proportion of patients with non-fatal cardiac arrest

    Time frame: Within 30 days of randomization

  4. Proportion of patients who require hospitalization for heart failure

    Time frame: Within 30 days of randomization

  5. Proportion of patients who develop pulmonary embolism and/or deep vein thrombosis

    Time frame: Within 30 days of randomization

  6. Proportion of patients with International Society on Thrombosis and Haemostasis (ISTH) major bleeding

    Time frame: Within 30 days of randomization

  7. Proportion of patients with bleeding independently associated with mortality following noncardiac surgery (BIMS)

    Time frame: Within 30 days of randomization

  8. Proportion of patients with infection or sepsis

    Time frame: Within 30 days of randomization

  9. Proportion of patients with acute renal failure fulfilling Kidney Disease Improving Global Outcomes (KDIGO) criteria

    Time frame: Within 30 days of randomization

  10. Proportion of patients with acute renal failure requiring dialysis

    Time frame: Within 30 days of randomization

  11. Proportion of patients requiring amputation

    Time frame: Within 30 days of randomization

  12. Mean length of stay

    Time frame: During index hospitalization up to 3 days

  13. Mean length of intensive care unit stay

    Time frame: During index hospitalization up to 1 week

  14. Mean days alive without need for intensive care support

    Time frame: During index hospitalization up to 3 days

Study contacts

Contact information is provided by the study sponsor or research team.

Chun Ka Wong, Clinical Assistant Professor

CONTACT

[email protected]

+852 2255 3597

Lily Hung, Master

CONTACT

[email protected]

+852 2255 4169

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Collaborators

  • Research Grants Council, Hong Kong

Registry information

Official study title

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

Acronym: GLUMINS

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Mar 22, 2024
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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