Staged Complete Revascularization for Coronary Artery Disease vs Medical Management Alone in Patients With AS Undergoing Transcatheter Aortic Valve Replacement (NCT04634240)
A Randomized, Comparative Effectiveness Study of Staged Complete Revascularization With Percutaneous Coronary Intervention to Treat Coronary Artery Disease vs Medical Management Alone in Patients With Symptomatic Aortic Valve Stenosis Undergoing Elective Transfemoral Transcatheter Aortic Valve Replacement: The COMPLETE TAVR Study
π©Ί Plain-English Summary (8th-Grade Level)
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 β₯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.
Who can join: Review the eligibility criteria below.
Location: Huntsville Heart Center β Huntsville, Alabama
π§ͺ Interventions in This Study
- Percutaneous Coronary Intervention (PCI) (PROCEDURE)
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (72 Sites)
Showing the first 25 of 72 sites.
- Huntsville Heart Center β Huntsville, Alabama
- Arizona Cardiovascular Research β Phoenix, Arizona
- Veteran Affairs Palo Alto Health Care System β Palo Alto, California
- Loma Linda University β Redlands, California
- Santa Barbara Cottage Hospital β Santa Barbara, California
- Torrance Memorial Medical Center β Torrance, California
- JFK Medical Center β Atlantis, Florida
- Baptist Health Jacksonville β Jacksonville, Florida
- Miami Cardiac and Vascular/Baptist Hospital β Miami, Florida
- Piedmont β Atlanta, Georgia
- Northeast Georgia Health System β Gainesville, Georgia
- St. Alphonsus Regional Medical Center β Boise, Idaho
- Ascension Alexian Brothers β Chicago, Illinois
- Midwest Cardiovascular Research and Education Foundation β Elkhart, Indiana
- Parkview Research Center β Fort Wayne, Indiana
- University of Kansas Medical Center β Kansas City, Kansas
- Midwest Heart and Vascular β Overland Park, Kansas
- Cardiovascular Research Institute of Kansas β Wichita, Kansas
- Tufts Medical β Boston, Massachusetts
- Massachusetts General Hospital β Boston, Massachusetts
- Sparrow Clinical Research Institute β Lansing, Michigan
- William Beaumont Hospital β Royal Oak, Michigan
- Ascension St. Mary's β Saginaw, Michigan
- St. Joseph Mercy Health System β Ypsilanti, Michigan
- University of Minnesota Medical Center β Minneapolis, Minnesota
π Contact the Study Coordinator
Phone: (604) 875-4111
Email: brobinson@cci-cic.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
π° Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Aortic Stenosis
- PERIGON Pivotal Trial β Los Angeles, California
- ACURATE IDE: Safety and Effectiveness Study of ACURATE Valve for Transcatheter Aortic Valve Replacement β Birmingham, Alabama
- PARTNER 3 Trial: Safety and Effectiveness of the SAPIEN 3 Transcatheter Heart Valve in Low Risk Patients With Aortic Stenosis β Birmingham, Alabama
- Use of DurAVRβ’ THV System in Subjects With Severe Aortic Stenosis: Early Feasibility Study β Tucson, Arizona
- Application of TAVI at Experienced Interventional Cardiac Centers Without On-site Cardiac Surgery (ATLAS Study) β Edmonton, Alberta
- Systematic Ambulatory ECG Monitoring Following TAVI β QuΓ©bec, Quebec
Explore by condition: All Aortic Stenosis clinical trials
π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.