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Clinical Trials/NCT02127996
NCT02127996
Unknown
Phase 2

A Study to Investigate the Protective Effects of Glucagon-like Peptide-1 (GLP-1) in Patients Undergoing Elective Angioplasty and Stenting (GOLD-PCI)

Papworth Hospital NHS Foundation Trust1 site in 1 country193 target enrollmentMarch 2015

Overview

Phase
Phase 2
Intervention
placebo
Conditions
Angina Pectoris
Sponsor
Papworth Hospital NHS Foundation Trust
Enrollment
193
Locations
1
Primary Endpoint
Plasma Troponin I level
Last Updated
7 years ago

Overview

Brief Summary

Angina is caused by narrowings or blockages within coronary arteries. Coronary angioplasty and stenting is performed for people with angina to improve the blood supply to the heart by placing metal tubes within the artery using balloon inflation. The procedure risks small but significant damage to the heart muscle downstream of the balloon.

Glucagon like peptide 1 (GLP 1) is a naturally occurring hormone secreted by cells in the gut in response to food. It acts by stimulating the release of insulin. In the heart it acts to increase glucose uptake into cardiac muscle. GLP-1 can protect the heart and improve heart muscle performance in people with coronary artery disease in physiological studies. This study which assesses whether GLP-1 protects the heart during coronary angioplasty and stenting.

The hypothesis is that GLP-1 given during elective coronary angioplasty and stenting will reduce cardiac troponin rise (a measure of heart muscle damage) compared to placebo.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
July 2021
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Normal Saline

Infusion of Normal Saline during Percutaneous Coronary Intervention

Intervention: placebo

GLP-1

Infusion of GLP-1 (7-36) amide during elective percutaneous coronary intervention

Intervention: GLP-1

Outcomes

Primary Outcomes

Plasma Troponin I level

Time Frame: 6 Hours following angioplasty or stenting

Incidence of Troponin I elevation of \> 5 x 99th percentile upper reference limit on blood test at approximately 6 hours post procedure.

Secondary Outcomes

  • Electrocardiographic (ECG) Changes during procedure(Assessed during procedure)
  • Ischaemic symptoms during balloon occlusion(Assessed during procedure)
  • Major Adverse Cardiovascular or Cerebrovascular Event (MACCE) Rates(From date of randomisation until the date of first event assessed up to 6 months)
  • Plasma Creatine Kinase - Myocardial Bound (CKMB) level(6 hours)
  • Myocardial Flow Grade after Angioplasty or Stenting(Measured during procedure)
  • MACCE Rates(From date of randomisation until the date of first event assessed up to 60 months)
  • Myocardial Blush Grade following angioplasty or stenting(Measured during procedure)

Study Sites (1)

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