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NCT03217006NARecruiting

Randomization of Single vs Multiple Arterial Grafts

Weill Medical College of Cornell University

Start Date

1/7/2018

Completion Date

1/1/2030

Summary

The primary hypothesis of ROMA is that in patients undergoing primary isolated non-emergent coronary artery bypass surgery (CABG), the use of two or more arterial grafts compared to a single arterial graft is associated with a reduction in the composite outcome of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The secondary hypothesis is that in patients undergoing primary isolated non-emergent CABG, the use of two or more arterial grafts compared to a single arterial graft is associated with improved survival. Prospective event-driven unblinded randomized multicenter trial of at least 4,300 subjects enrolled in at least 25 international centers. Patients will be randomized to a single arterial graft (SAG) or multiple arterial grafts (MAG). Patients will be randomized in a 1:1 fashion between the two groups. Permuted block randomization with random blocks stratified by the center and the type of second arterial graft will be used to provide treatment distribution in equal proportion.

Detailed Description

In the 1980's, it was recognized that long-term survival was enhanced in patients undergoing coronary surgery when the left anterior descending (LAD) was grafted with a left internal thoracic artery (ITA) rather than a saphenous vein (1). This difference was predicated, at least in part, due to greater and more durable patency of the left ITA compared to an increased early occlusion rate and later progressive atherosclerosis of saphenous vein grafts (SVG) (2). For more than 20 years it has generally been accepted that patients who receive multiple arterial grafts (AGs) at the time of coronary artery bypass surgery (CABG) have increased postoperative survival compared to those who receive only one AG, especially over the long term (3-5). The current United States and European Guidelines encourage the use of AGs in patients with a long life expectancy (6, 7). Last year, a position paper from the Society of Thoracic Surgeons strongly recommended a wider use of AGs (8). The putative mechanism underlying the AG hypothesis is greater patency. In line with the original findings of improved LAD graft patency with ITA vs. SVG, data from randomized control trials (RCTs) as well as observational studies and a network meta-analysis (9) have demonstrated that the patency of the RA, as well as the right ITA, exceed that of a SVG, providing mechanistic basis to support the AG hypothesis. ROMA is a two arm event driven randomized multi-centre trial aimed at evaluating the impact of the use of one ITA vs two or more AGs for CABG on a composite of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The trial is powered to detect a 20% relative reduction in the primary outcome with 90% power at 5% alpha. The primary aim is to conduct a multicenter international randomized control trial to test the hypothesis that the use of a two or more AGs compared to a single arterial graft is associated with a reduction in the composite outcome of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The secondary aim is to conduct a multicenter international randomized control trial to test the hypothesis that the use of two or more AGs compared to a single arterial graft is associated with improved survival.

Eligibility Criteria

Age Range: 18 years to 70 years

Inclusion Criteria: * Primary isolated CABG patients with disease of the left main coronary artery and/or of the left anterior descending and the circumflex coronary system with or without disease of the right coronary artery. Exclusion Criteria: * Age \> 70 years * Single graft * Emergency operation * Evolving myocardial infarction within 48 hours of surgery * Left ventricular ejection fraction of \< 35% * Any concomitant cardiac or non-cardiac procedure * Previous cardiac surgery * Preoperative severe end-organ dysfunction (dialysis, liver failure, respiratory failure), cancer or any co-morbidity that reduce life expectancy to less than 5 years. * Inability to use the saphenous vein or to use both radial and right internal thoracic arteries * Anticipated need for coronary thrombo-endarterectomy * Planned hybrid revascularization

Interventions

PROCEDURE

Single arterial graft

PROCEDURE

Multiple arterial grafting

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Conditions

Coronary Artery DiseaseHeart Diseases

Locations

University of Colorado

Boulder, Colorado 80309

United States

Baystate Health

Springfield, Massachusetts 01109

United States

Nebraska Heart Hospital

Lincoln, Nebraska 68526

United States

University of Nebraska Medical Center

Omaha, Nebraska 68198

United States

NewYork-Presbyterian Brooklyn Methodist Hospital

Brooklyn, New York 11215

United States

Icahn School of Medicine, Mount Sinai

New York, New York 10029

United States

Weil Cornell Medical College Department of Cardiothoracic Surgery

New York, New York 10065

United States

Lenox Hill Hospital (Northwell)

New York, New York 10075

United States

NewYork-Presbyterian Queens

New York, New York 11355

United States

Cleveland Clinic Foundation

Cleveland, Ohio 44106

United States

Allegheny General Hospital (Cardiovascular Institute)

Pittsburgh, Pennsylvania 15232

United States

Innsbruck (Medical University) Austria

Innsbruck,

Austria

Krankenhaus Nord Vienna North Hospital

Vienna,

Austria

MU Vienna Austria

Vienna,

Austria

Federal University of Sao Paulo

São Paulo,

Brazil

Hamilton General Hospital

Hamilton,

Canada

London Health Sciences Ontario Canada

London,

Canada

University Hospital of Montreal (CHUM)

Montreal,

Canada

University of Ottawa Heart Institute Canada

Ottawa,

Canada

Royal Victoria Hospital (McGill)

Québec,

Canada

Universite Laval Quebec (CRIUCPQ) Canada

Québec,

Canada

Sunnybrook Health Sciences Centre

Toronto,

Canada

Toronto General Hospital

Toronto,

Canada

St. Boniface General Hospital / WHRA

Winnipeg,

Canada

Fuwai Hospital

Beijing,

China

Jilin Heart Hospital

Changchun,

China

Ruijin Hospital Shanghai Jiao Tong University School of Medicine

Shanghai,

China

National Taiwan University Hospital

Taiwan,

China

Teda Hospital (TICH)

Tianjin,

China

University Hospital Dubrava

Zagreb,

Croatia

General University Hospital, Prague

Prague,

Czechia

Duisburg Heart Center

Duisburg,

Germany

Essen University

Duisburg,

Germany

Düsseldorf University

Düsseldorf,

Germany

University Hospital Erlangen

Erlangen,

Germany

Giessen Hospital

Giessen,

Germany

University Medical Center of Goettingen

Göttingen,

Germany

Jena University Hospital

Jena,

Germany

Heart Center (Herzzentrum)

Leipzig,

Germany

HDZ NRW Bad

Oeynhausen,

Germany

Robert-Bosch-Hospital

Stuttgart,

Germany

Krankenhaus der Barmherzigen Brüder Trier

Trier,

Germany

Anthea Hospital

Bari,

Italy

Fondazione Poliambulanza

Brescia,

Italy

Maria Cecilia Hospital GVM

Cotignola,

Italy

Universita' Cattolica del Sacro Cuore

Roma,

Italy

European Hospital

Rome,

Italy

Ospedale Le Molinette

Torino,

Italy

Saitama Medical University

Saitama,

Japan

MUMC Maastricht (University Medical Centre)

Maastricht,

Netherlands

Medical University of Silesia (Katowice)

Katowice,

Poland

Hospitalar de Lisboa Central

Capuchos,

Portugal

University Hospital (Praceta Mota Pinto)

Coimbra,

Portugal

Centro Hospitalar e Universitário São João

Porto,

Portugal

Dedinje Cardiovascular Institute

Belgrade,

Serbia

National University of Singapore

Singapore,

Singapore

Severance Cardiovascular Hospital, Yonsei University College of Medicine

Sinchŏn-dong,

South Korea

Hospital Univeritario Del Vinalopo

Alicante,

Spain

Hospital Clinic de Barcelona (ICCV)

Barcelona,

Spain