Trial Evaluating New Strategy in the Functional Assessment of 3-vessel Disease Using SYNTAXII Score in Patients With PCI

European Cardiovascular Research Institute (ECRI)

Status

Completed

Conditions

3 Vessel Coronary Artery Disease

Cardiovascular Diseases

Heart Diseases

Treatments

Device: Intravascular Ultrasound

Device: Fractional flow reserve

Device: Coronary stent

Device: instantaneous wave-free ratio

Radiation: Multi Slice Computed Tomography

Study type

Observational

Funder types

Industry

Identifiers

NCT02015832

ECRI-002

Details and patient eligibility

About

Clinical study that aims to evaluate a new strategy using the SYNTAX II Score calculator in the functional assessment of patients with new coronary 3-vessel-disease who undergo percutaneous coronary intervention (PCI)

Full description

The purpose of the SYNTAX II Trial is to investigate the management of de-novo 3-vessel-disease in order to prospectively assess which patients would have at least comparable short and long term clinical outcomes between coronary artery bypass graft and percutaneous coronary intervention (PCI), using contemporary PCI practice. In SYNTAX II the effectiveness of a contemporary stent (designed with thinner struts, biocompatible and biodegradable polymer, and a limus based drug), the use of pressure wire assessment of lesions to allow for ischemia-driven revascularisation, intravascular ultrasound (IVUS) guidance to optimise drug eluting stent deployment, and the treatment of (chronic) total occlusion lesions with contemporary techniques, will be compared against PCI practice in the original SYNTAX trial. The proposed study would involve the SYNTAX Score II to prospectively recruit subjects on the grounds of patient safety

Enrollment

454 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

At least 1 stenosis, angiographic, visually determined de novo lesions with more than 50 percent diameter stenosis in all 3 major epicardial territories. These are left descending coronary artery (LAD) and or side branch, proximal circumflex coronary artery (LCX) and or side branch, right descending coronary artery (RCA) and or side branch which are supplying viable myocardium without left main involvement. Patients with ostial LAD or ostial CX Medina 0,0,1 or Medina 0,1,0 may be enrolled
Patients with hypoplastic RCA with absence of descending posterior and presence of a lesion in the LAD and CX territories may be included in the trial as a 3 vessel disease equivalent
Vessel size should be at least 1.5 mm in diameter as visually assessed in diagnostic angiogram
Patients with
1. stable (Canadian Cardiovascular Society Class 1, 2, 3 or 4) angina pectoris
2. or unstable (Braunwald class) angina pectoris and ischemia
3. or patients with atypical chest pain or those who are asymptomatic provided they have myocardial ischemia, for example treadmill exercise test, radionuclide scintigraphy, stress echocardiography
All anatomical SYNTAX Scores are eligible for initial screening with the SYNTAX Score II
Patient has been informed of the nature of the study and agrees to its provisions and has provided written informed consent as approved by the Ethical Committee of the respective clinical site
Signed Heart Team Decision Form between local cardiologist and surgeon that the selected case meets all of the inclusion and exclusion criteria

Exclusion criteria

Under the age of 21 years
Known pregnancy at time of enrolment. Female of childbearing potential, and last menstruation within the last 12 months, who are not taking adequate contraceptives. Female who is breastfeeding at time of enrolment
Prior PCI or CABG
Ongoing acute myocardial infarction and enzymes (CKMB) more than 2x upper limit of normal
Concomitant cardiac valve disease requiring surgical therapy, reconstruction or replacement
Single or two-vessel disease at time of Heart Team consensus
Participation or planned participation in another cardiovascular clinical study before one year follow up is completed
Mental condition, psychiatric or organ cerebral disease, rendering the subject unable to understand the nature, scope, and possible consequences of the study or mental retardation or language barrier such that the patient is unable to give informed consent and potential for non-compliance towards the requirement in the study protocol