Coronary Plaque Geometry and Acute Coronary Syndromes

NCT ID: NCT03702764

Last Updated: 2022-08-02

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 1000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-02-01
• Study Completion Date: 2021-11-30

Brief Summary

The aim of GEOMETRY study is to investigate the correlation between coronary plaque geometric modifications and lesion vulnerability in patients with suspected coronary artery disease referred for cardiac computed tomography angiography (CCTA). Furthermore the study will evaluate the impact of plaque eccentricity and morphology on the rate of major adverse cardiovascular events (MACE) for a 2 years follow-up period.

Detailed Description

Coronary artery disease (CAD) remains the leading cause of mortality and morbidity worldwide. Early detection of CAD may reduce the incidence of myocardial infarction by improving primary prevention and providing more effective treatment methods. A step in this direction is identifying the pattern of coronary plaques which are prone to rupture. Coronary computed tomography angiography (CCTA) has emerged recently as a reliable noninvasive tool used in the evaluation of coronary arteries. Some features related to plaque composition and morphology such as low attenuation plaques, spotty calcification, positive remodeling or napkin ring sign, were already identified as vulnerability markers. However the role of lesion geometry on plaque vulnerability was not investigated yet.

This is a prospective, cohort, single-center study which will be carried out in the Center of Advanced Research in Multimodal Cardiac Imaging Cardiomed.

The study will include 1.000 subjects with suspected CAD who are referred to CCTA by the attending physician and in which presence of at least one coronary plaque is confirmed by CCTA.

Plaque burden, composition, and morphology will be assessed for each plaque. Longitudinal and transversal eccentricity will be also assessed in each plaque and in all cases, eccentricity index will be calculated in cross-section plane at the degree of maximum stenosis in order to determine the position of the remaining circulant lumen and to classify the plaque into concentric and eccentric lesion.

The study will be conducted over a period of 3 years, in which patients will be examined at baseline, and will be followed-up for 2 years for occurrence of MACE.

Study objectives:

Primary: to evaluate the association between different patterns of plaque geometry and the risk for major adverse cardiac events MACE (all-cause mortality, cardiovascular death, myocardial infarction, repeated revascularization, repeated hospitalizations for cardiovascular related incidents, cerebrovascular events) during a 2-year follow-up, Secondary: to evaluate the association of plaque eccentricity, plaque vulnerability and plaque progression after 2 years of follow-up

Study Timeline:

• Baseline (day 0)

• Obtain and document consent from participant on study consent form.
• Verify inclusion/exclusion criteria.
• Obtain demographic information, medical history, medication history, alcohol and tobacco use history.
• Record results of physical examinations and 12-lead ECG.
• Collect blood specimens.
• Imaging: 128-multislice CT angiography.
• Visit 1 (month 6)

• Record results of physical examinations, 12-lead ECG and medical history.
• MACE assessment
• Visit 2 (month 12)

• Record results of physical examinations, 12-lead ECG and medical history.
• MACE assessment
• Visit 3 (month 18)

• Record results of physical examinations, 12-lead ECG and medical history.
• MACE assessment
• Final study visit (month 24)

• Record results of physical examinations, 12-lead ECG and medical history.
• Repeat CCTA and plaque assessment
• End-point evaluation.

Study procedures:

• Medical history, clinical examination, laboratory tests;
• 12-lead ECG
• 128-multislice CT coronary angiography with the evaluation of: calcium score, plaque burden, markers for lesion severity (degree of stenosis, lesion length, lumen area and diameter, minimum and maximum plaque thickness); morphological plaque characteristics (plaque related volumes, plaque burden, remodeling indexes); shear stress by computational fluid dynamics; markers of plaque vulnerability (low attenuation plaque, spotty calcification, positive remodeling, napkin ring sign); plaque geometry by eccentricity index, longitudinal and transversal eccentricity.

Conditions

Coronary Stenosis; Acute Coronary Syndrome; Acute Myocardial Infarction; Atherosclerosis; Atheromatous Plaques

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

VP-SG 01

Study subjects that present concentric coronary plaques

CCTA

Intervention Type: DIAGNOSTIC_TEST

128-multislice CT coronary angiography and complex atherosclerotic plaque analysis, with the use of CT imaging post-processing techniques.

VP-SG 02

Study subjects that present eccentric coronary plaques

CCTA

Intervention Type: DIAGNOSTIC_TEST

128-multislice CT coronary angiography and complex atherosclerotic plaque analysis, with the use of CT imaging post-processing techniques.

Interventions

CCTA

128-multislice CT coronary angiography and complex atherosclerotic plaque analysis, with the use of CT imaging post-processing techniques.

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Patients with suspected coronary artery disease (CAD) and pre-test probability of CAD between 15% and 85%, who undergo CCTA, and in whom CCTA has identified presence of at least one coronary plaque
• Ability to provide informed consent
• Age grater then 18 years

Exclusion Criteria

• Patients with pre-test probability of CAD >85% or <15%
• Electrocardiographic evidence of STEMI
• Presence of pre-existing CAD including prior myocardial infarction
• History of coronary artery revascularization (by percutaneous coronary intervention, stent or bypass graft surgery)
• Atrial fibrillation or other irregular rhythm
• Unwillingness or incapacity to provide informed consent
• Allergy to iodine contrast media
• Inability to tolerate beta-blocker medication
• Renal insufficiency (creatinine greater than 1.5 mg/dL) or renal failure requiring dialysis
• Pregnant women or lactation
• Active malignancy or malignancy within the last 5 year prior to enrolment
• Conditions associated with an estimated life expectancy of under 2 years
• Coronary calcium score >1000

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Targu Mures, Romania

OTHER

Sponsor Role: collaborator

University Hospital of Targu Mures, Romania

OTHER

Sponsor Role: collaborator

Cardio Med Medical Center

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Cardio Med Medical Center

Târgu Mureş, Mureș County, Romania

Countries

Romania

Other Identifiers

CM0218-GEO

Identifier Type: -

Identifier Source: org_study_id