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NCT04634240NARecruiting

Staged Complete Revascularization for Coronary Artery Disease vs Medical Management Alone in Patients With AS Undergoing Transcatheter Aortic Valve Replacement

University of British Columbia

Start Date

12/19/2020

Completion Date

4/1/2026

Summary

Patients undergoing transcatheter aortic valve replacement (TAVR) often have concomitant coronary artery disease (CAD) which may adversely affect prognosis. There is uncertainty about the benefits and the optimal timing of revascularization for such patients. There is currently clinical equipoise regarding the management of concomitant CAD in patients undergoing TAVR. Some centers perform routine revascularization with percutaneous coronary intervention (PCI) (either before or after TAVR), while others follow an alternative strategy of medical management. The potential benefits and optimal timing of PCI in these patients are unknown. As TAVR expands to lower risk patients, and potentially becomes the preferred therapy for the majority of patients with severe aortic stenosis, the optimal management of concomitant coronary artery disease will be of increasing importance. The COMPLETE TAVR study will determine whether, on a background of guideline-directed medical therapy, a strategy of complete revascularization involving staged PCI using drug eluting stents to treat all suitable coronary artery lesions is superior to a strategy of medical therapy alone in reducing the composite outcome of Cardiovascular Death, new Myocardial Infarction, Ischemia-driven Revascularization or Hospitalization for Unstable Angina or Heart Failure. The study will be a randomized, multicenter, open-label trial with blinded adjudication of outcomes. Patients will be screened and consented for elective transfemoral TAVR and randomized within 96 hours of successful balloon expandable TAVR. Complete Revascularization: Staged PCI using third generation drug eluting stents to treat all suitable coronary artery lesions in vessels that are at least 2.5 mm in diameter and that are amenable to treatment with PCI and have a ≥70% visual angiographic diameter stenosis. Staged PCI can occur any time from 1 to 45 days post successful transfemoral TAVR. Vs. Medical Therapy Alone: No further revascularization of coronary artery lesions. All patients, regardless of randomized treatment allocation, will receive guideline-directed medical therapy consisting of risk factor modification and use of evidence-based therapies. The COMPLETE TAVR study will help address the current lack of evidence in this area. It will likely impact both the global delivery of health care and the management and clinical outcomes of all patients undergoing TAVR with concomitant CAD.

Eligibility Criteria

Age Range: No minimum to No maximum

Inclusion Criteria: \- Symptomatic aortic valve stenosis prior to TAVR (NYHA Functional Class ≥ 2 OR Abnormal exercise test with severe SOB, abnormal BP response, or arrhythmia) AND \- CAD defined as: at least 1 coronary artery lesion of ≥70% visual angiographic diameter stenosis in a native segment ≥2.5 mm in diameter that is not a CTO and is amenable to treatment with PCI AND \- Consensus by the Local Multidisciplinary Heart Team that the patient is suitable for elective transfemoral TAVR with a balloon expandable transcatheter heart valve AND would receive a bypass with an anastomosis distal to the coronary artery lesion(s) if they were undergoing SAVR. Local Multidisciplinary Heart Teams are expected to follow current clinical guidelines for selection of patients for TAVR with an eligible patient generally expected to have: \[AVA ≤ 1.0 cm2 OR AVA index ≤ 0.6 cm2/m2\] OR \[Jet velocity ≥ 4.0 m/s OR mean gradient ≥ 40 mmHg\] OR patients without these criteria may undergo TAVR if the Local Multidisciplinary Heart Team concludes it is appropriate. AND \- Successful transfemoral TAVR, defined as the implantation of a single transcatheter aortic valve within the past 96 hours with freedom from more than minimal aortic insufficiency, stroke, or major vascular complications. Exclusion Criteria: * PCI already performed within 90 days prior to TAVR or at the same time as the index transfemoral TAVR procedure * Planned PCI of coronary artery lesion(s) * Planned surgical revascularization of coronary artery lesion(s) * Non-cardiovascular co-morbidity reducing life expectancy to \< 5 years * Any factor precluding 5-year follow-up * Prior coronary artery bypass grafting surgery or surgical valve replacement * Severe mitral regurgitation (\> 3+) * Severe left ventricular dysfunction (LVEF \< 30%) * Low coronary takeoff (high risk for coronary obstruction) * Acute myocardial infarction within 90 days * Stroke or transient ischemic attack within 90 days * Renal insufficiency (eGFR \< 30 ml/min) and/or renal replacement Rx * Hemodynamic or respiratory instability

Interventions

PROCEDURE

Percutaneous Coronary Intervention (PCI)

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Conditions

Aortic StenosisCoronary Artery DiseaseCoronary Stenosis

Locations

Huntsville Heart Center

Huntsville, Alabama 35801

United States

Arizona Cardiovascular Research

Phoenix, Arizona 85027

United States

Veteran Affairs Palo Alto Health Care System

Palo Alto, California 94304

United States

Loma Linda University

Redlands, California 92373

United States

Santa Barbara Cottage Hospital

Santa Barbara, California 93105

United States

Torrance Memorial Medical Center

Torrance, California 90505

United States

JFK Medical Center

Atlantis, Florida 33462

United States

Baptist Health Jacksonville

Jacksonville, Florida 32207

United States

Miami Cardiac and Vascular/Baptist Hospital

Miami, Florida 33139

United States

Piedmont

Atlanta, Georgia 30309

United States

Northeast Georgia Health System

Gainesville, Georgia 30501

United States

St. Alphonsus Regional Medical Center

Boise, Idaho 83709

United States

Ascension Alexian Brothers

Chicago, Illinois 60007

United States

Midwest Cardiovascular Research and Education Foundation

Elkhart, Indiana 46514

United States

Parkview Research Center

Fort Wayne, Indiana 46845

United States

University of Kansas Medical Center

Kansas City, Kansas 66160

United States

Midwest Heart and Vascular

Overland Park, Kansas 66211

United States

Cardiovascular Research Institute of Kansas

Wichita, Kansas 64131

United States

Tufts Medical

Boston, Massachusetts 02111

United States

Massachusetts General Hospital

Boston, Massachusetts 02114

United States

Sparrow Clinical Research Institute

Lansing, Michigan 48912

United States

William Beaumont Hospital

Royal Oak, Michigan 48073

United States

Ascension St. Mary's

Saginaw, Michigan 48197

United States

St. Joseph Mercy Health System

Ypsilanti, Michigan 48197

United States

University of Minnesota Medical Center

Minneapolis, Minnesota 55455

United States

CentraCare Heart and Vascular Center

Saint Cloud, Minnesota 56303

United States

Boone Hospital

Columbia, Missouri 65201

United States

St. Louis University

St Louis, Missouri 63103

United States

Missouri Baptist

St Louis, Missouri 63131

United States

Bryan Heart

Lincoln, Nebraska 68506

United States

Dartmouth Hitchcock Medical Center

Lebanon, New Hampshire 03765

United States

Our Lady of Lourdes

Camden, New Jersey 08103

United States

Valley Hospital

Ridgewood, New Jersey 07450

United States

University at Buffalo

Buffalo, New York 14203

United States

NYU Langone Hospital - Long Island

Mineola, New York 11501

United States

Mount Sinai

New York, New York 10029

United States

Columbia University Medical Center

New York, New York 10552

United States

St. Joseph's Hospital

Syracuse, New York 13088

United States

Montefiore Medical Center

The Bronx, New York 10467

United States

Novant Health Heart and Vascular Institute

Charlotte, North Carolina 28204

United States

Summa Health System

Akron, Ohio 44304

United States

Mount Carmel

Columbus, Ohio 43213

United States

Oklahoma Heart

Oklahoma City, Oklahoma 73110

United States

Kaiser Permanente Northwest

Clackamas, Oregon 97015

United States

Rhode Island Hospital

Providence, Rhode Island 02903

United States

Methodist Le Bonheur Healthcare

Germantown, Tennessee 38138

United States

Ballad Health CVA Heart Institute

Kingsport, Tennessee 37660

United States

Parkwest Medical Center

Knoxville, Tennessee 37923

United States

Cardiovascular Surgery Clinic/Baptist Memorial

Memphis, Tennessee 38671

United States

HCA Houston Healthcare Medical Center

Houston, Texas 77004

United States

Baylor Scott & White Plano

Plano, Texas 75093

United States

Baylor Scott & White Round Rock

Round Rock, Texas 78665

United States

University of Vermont Medical Center

Burlington, Vermont 05401

United States

Bellin Health System

Green Bay, Wisconsin 54301

United States

Ascension Columbia St. Mary's

Milwaukee, Wisconsin 53211

United States

University of Alberta, Mazankowski Heart Institute

Edmonton, Alberta T6G 2B7

Canada

Royal Columbian Hospital

New Westminster, British Columbia V3L 3W7

Canada

Vancouver General Hospital

Vancouver, British Columbia V5Z 1M9

Canada

Centre for Cardiovascular Innovation-Centre d'Innovation Cardiovasculaire (CCI-CIC)

Vancouver, British Columbia V5Z1M9

Canada

St. Paul's Hospital

Vancouver, British Columbia V6Z 1Y6

Canada

Saint Boniface

Winnipeg, Manitoba R2H 2A6

Canada

New Brunswick Heart

Saint John, New Brunswick E2L 4L2

Canada

Queen Elizabeth II Health Sciences Centre

Halifax, Nova Scotia B3H 3A7

Canada

Hamilton Health Sciences

Hamilton, Ontario L8L 2X2

Canada

Ottawa Heart

Ottawa, Ontario K1Y 4W7

Canada

Sunnybrook Hospital

Toronto, Ontario M4N 3M5

Canada

St. Michael's Hospital

Toronto, Ontario M5B 1W8

Canada

Montréal Heart

Montreal, Quebec H1T 1C8

Canada

Centre Hospitalier de l'Université de Montréal

Montreal, Quebec H2X 3E4

Canada

Sacré-Coeur

Montreal, Quebec H4J 1C4

Canada

CIUSSS de l'Estrie-CHUS

Sherbrooke, Quebec J1H 5H3

Canada

Prairie Vascular

Regina, Saskatchewan S4P 0W5

Canada