Coronary Artery Disease Progression in Patients With Prediabetes
Primary Purpose
Coronary Artery Disease, Atherosclerosis, Prediabetic State
Status
Completed
Phase
Phase 4
Locations
Latvia
Study Type
Interventional
Intervention
Metformin
Lifestyle recommendations
Sponsored by
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Coronary artery disease, Atherosclerosis, Prediabetes, Intravascular ultrasound, Insulin resistance, Percutaneous coronary intervention, Metformin
Eligibility Criteria
Inclusion Criteria:
- age ≥18 and <75 years;
- patients with stable coronary artery disease referred to PCI in an artery suitable for IVUS pullback;
- signed informed consent before PCI.
Exclusion Criteria:
- cardiac or non-cardiac illness with life expectancy of less than two years;
- failure to advance the IVUS catheter through the culprit lesion;
- acute coronary syndrome
- congestive heart failure (New York Heart Association (NYHA) classification stage III-IV)
- diabetes mellitus
- chronic kidney disease
- previous PCI in the target vessel
- heavily calcified vessels
- allergy to metformin
Sites / Locations
- Pauls Stradins Clinical University hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Prediabetes, metformin
Prediabetes, lifestyle
Arm Description
Patients with HbA1c 5.7-6.4 receiving metformin and lifestyle recommendations
Patients with HbA1c 5.7-6.4 receiving lifestyle recommendations
Outcomes
Primary Outcome Measures
Percentage plaque volume change over 24 months
Changes in plaque volume in 24 months
Secondary Outcome Measures
Culprit lesion in-stent restenosis
Neointimal hyperplasia at 24 month follow up
Plaque tissue component percentage change over 24 months
Percentage change in necrotic, fibrotic, lipidic and calcific tissue volume
Correlation of glycemic parameters with plaque characteristics
Correlation of glycemic parameters with plaque characteristics
Plaque volume change in metformin vs non-metformin treated patients over 24 months
Plaque volume change in metformin vs non-metformin treated patients over 24 months
Full Information
NCT ID
NCT02744976
First Posted
April 15, 2016
Last Updated
April 21, 2022
Sponsor
Pauls Stradins Clinical University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02744976
Brief Title
Coronary Artery Disease Progression in Patients With Prediabetes
Official Title
Coronary Artery Disease Progression by iMap Intravascular Ultrasound Analysis in Patients With Prediabetes
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
February 2016 (undefined)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
September 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pauls Stradins Clinical University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Prediabetes is a disorder of glucose metabolism that reflects the natural history of progression from normoglycaemia to type 2 diabetes mellitus. Patients with prediabetes have impaired glucose regulation caused by insulin resistance (IR). IR in patients undergoing percutaneous coronary intervention (PCI) is associated with coronary artery remodeling and coronary plaque vulnerability by intravascular ultrasound (IVUS) analysis. In stent restenosis after bare metal and drug-eluting stent implantation more frequently is observed in patients with high fasting-insulin levels and IR. Although IR has a significant role in the progression of atherosclerosis in prediabetic patients, the importance of managing prediabetes is often under-appreciated by clinicians. To date, no pharmacological treatment has been officially approved for prediabetes. According to American Diabetes Association recommendations, metformin is the only drug that could be considered in the treatment of prediabetic patients with a high risk of developing diabetes. Metformin is a safe and inexpensive glucose lowering drug that attenuates mortality and future cardiovascular events in patients with type 2 diabetes as well as the progression of atherosclerosis in non-diabetic animal models. This study was designed to analyze coronary plaque characteristics by iMAP IVUS in patients with and without prediabetes undergoing PCI and to evaluate the impact of metformin treatment on coronary plaque characteristics in prediabetic patients at 24 month follow up.
The study hypothesis is that more pronounced coronary atherosclerosis progression as well as in-stent neointimal hyperplasia will be observed in patients with prediabetes. Metformin treatment attenuates the progression of atherosclerosis in patients with prediabetes.
Detailed Description
Patients undergoing PCI and IVUS pullback for the target vessel will be enrolled in a prospective study. Before PCI and at 24 month follow up fasting blood will be collected for glucose, HbA1c, C peptide, lipid profile assessment. Patients' baseline demographic characteristics, medical history, and procedural data will be collected during the index hospitalization and at 24 month follow up. Patients will be divided in groups according to HbA1c - control group (HbA1c<5.7) and prediabetic patients (HbA1c 5.7-6.4). PCI will be performed in accordance with the guidelines. After successful treatment of the culprit lesion IVUS will be done. Following PCI and IVUS patients with prediabetes will be randomly assigned in groups either receiving metformin at a dose of 2000 mg once daily plus standard lifestyle recommendations or standard lifestyle recommendations only. Intravascular ultrasound analysis will be repeated 24 months after the initial PCI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Atherosclerosis, Prediabetic State
Keywords
Coronary artery disease, Atherosclerosis, Prediabetes, Intravascular ultrasound, Insulin resistance, Percutaneous coronary intervention, Metformin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Prediabetes, metformin
Arm Type
Experimental
Arm Description
Patients with HbA1c 5.7-6.4 receiving metformin and lifestyle recommendations
Arm Title
Prediabetes, lifestyle
Arm Type
Active Comparator
Arm Description
Patients with HbA1c 5.7-6.4 receiving lifestyle recommendations
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glucophage extended release (XR)
Intervention Description
In order to minimize gastrointestinal discomfort, metformin treatment will be started with a dose of 500 mg p/o once daily, then gradually increased to 2000 mg p/o once daily for 24 months
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle recommendations
Intervention Description
Standard lifestyle recommendations
Primary Outcome Measure Information:
Title
Percentage plaque volume change over 24 months
Description
Changes in plaque volume in 24 months
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Culprit lesion in-stent restenosis
Description
Neointimal hyperplasia at 24 month follow up
Time Frame
24 months
Title
Plaque tissue component percentage change over 24 months
Description
Percentage change in necrotic, fibrotic, lipidic and calcific tissue volume
Time Frame
24 months
Title
Correlation of glycemic parameters with plaque characteristics
Description
Correlation of glycemic parameters with plaque characteristics
Time Frame
At index hospitalization and follow up (24 months)
Title
Plaque volume change in metformin vs non-metformin treated patients over 24 months
Description
Plaque volume change in metformin vs non-metformin treated patients over 24 months
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age ≥18 and <75 years;
patients with stable coronary artery disease referred to PCI in an artery suitable for IVUS pullback;
signed informed consent before PCI.
Exclusion Criteria:
cardiac or non-cardiac illness with life expectancy of less than two years;
failure to advance the IVUS catheter through the culprit lesion;
acute coronary syndrome
congestive heart failure (New York Heart Association (NYHA) classification stage III-IV)
diabetes mellitus
chronic kidney disease
previous PCI in the target vessel
heavily calcified vessels
allergy to metformin
Facility Information:
Facility Name
Pauls Stradins Clinical University hospital
City
Riga
Country
Latvia
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Coronary Artery Disease Progression in Patients With Prediabetes
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