Coronary Artery Disease Clinical Trials
51 studies are recruiting for coronary artery disease in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Product Surveillance Registry
The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by str…
- Stage
- Not phased
- Ages
- Any age
- Site
- Research site, Birmingham, Alabama
- Locations
- 401 in total
- Run by
- Medtronic
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Factors Affect Outcomes in Cardiovascular Surgery
Identify factors that contribute to perioperative morbidity and mortality in patients undergoing cardiac surgery that involves cardiopulmonary bypass. Identify factors that affect perioperative morbidity and mortality in patients undergoing cardiac surgery.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of California Davis Health System, Sacramento, California
- Run by
- University of California, Davis
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Hyperpolarized 13C Pyruvate-MRI and FDG-PET in a Single Exam for the Prognosis of Ischemic Cardiomyopathy
This prospective, non-blinded, single-center, translational research study aims to validate a multimodal advanced imaging exam for cardiac viability. The protocol utilizes three distinct imaging modalities: Single Photon Emission Computed Tomography Myocardial Perfusion Imaging (SPECT MPI), 18F-flu…
- Stage
- Not phased
- Ages
- 20 to 80
- Site
- University of Texas Southwestern Medical Center, Dallas, Texas
- Run by
- University of Texas Southwestern Medical Center
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Prognostic Value of Hyperpolarized 13C MRI for Clinical Myocardial Viability
Heart failure due to coronary artery disease represents a significant cause of mortality. The detection of patients eligible for bypass surgery is a pivotal concern. Nevertheless, the optimal approach for patient selection based on conventional imaging scans remains unclear. The proposed method (Hy…
- Stage
- Not phased
- Ages
- 20 to 80
- Site
- University of Texas Southwestern Medical Center, Dallas, Texas
- Run by
- University of Texas Southwestern Medical Center
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Investigational Trial to Evaluate XC001 Delivered Via an Cardiac Catheter in Subjects With Chronic Angina.
This is a two-part study, comprised of an initial open-label run-in phase (Part 1) in a subset of 3 subjects to provide first data regarding safety, and feasibility of the percutaneous endovascular catheter-facilitated intramyocardial delivery of XC001 in patients with RA due to obstructive CAD. Pa…
- Stage
- Phase 2
- Ages
- 18 to 85
- Site
- Alabama Cardiology PC, Birmingham, Alabama
- Locations
- 14 in total
- Run by
- XyloCor Therapeutics, Inc.
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Pivotal Study of the SUpira System in Patients Undergoing High-Risk Percutaneous COronaRy InTervention (HRPCI)
The objective of this study is to assess the safety and efficacy of the Supira System in providing temporary cardiovascular hemodynamic support in patients undergoing HRPCI. Eligible patients will be randomized to undergo HRPCI with either the Supira System (investigational device) or the commercia…
- Stage
- Not phased
- Ages
- 18 to 90
- Site
- Loma Linda University Medical Center, Loma Linda, California
- Locations
- 19 in total
- Run by
- Supira Medical
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Influence of Pulse Electromagnetic Field Therapy on Myocardial Ischemia
This study is being done to observe the effects of treatment from a device called the Bioboosti which utilizes pulsed electromagnetic waves on its ability to improve blood flow to the heart tissue in individuals with coronary artery disease (CAD).
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mayo Clinic in Arizona, Scottsdale, Arizona
- Locations
- 2 in total
- Run by
- Mayo Clinic
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A Phase 2b Clinical Trial of YN001 in Adults With Coronary Atherosclerosis
This study is designed to evaluate the efficacy and safety of intravenously administered YN001 in patients diagnosed with coronary atherosclerosis, who are receiving background therapy for cardiovascular (CV) risk factors management.
- Stage
- Phase 2
- Ages
- 18 to 80
- Site
- Washington University School of Medicine, St Louis, Missouri
- Locations
- 40 in total
- Run by
- Beijing Inno Medicine Co., Ltd.
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REvascularization CHoices Among Under-Represented Groups Evaluation: The RECHARGE Trial - Women
This is a research study in women to compare the outcomes of two procedures that restore blood flow to the arteries of the heart. In one procedure the blockages are ballooned and then stented with a small wire mesh tube through a small incision in the wrist or the groin. The other procedure is an o…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Adventist Health Glendale, Glendale, California
- Locations
- 18 in total
- Run by
- Weill Medical College of Cornell University
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REvascularization CHoices Among Under-Represented Groups Evaluation: The RECHARGE Trial - Minorities
This is a research study in minorities to compare the outcomes of two procedures that restore blood flow to the arteries of the heart. In one procedure the blockages are ballooned and then stented with a small wire mesh tube through a small incision in the wrist or the groin. The other procedure is…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Adventist Health Glendale, Glendale, California
- Locations
- 18 in total
- Run by
- Weill Medical College of Cornell University
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A Prospective, Multicenter, Randomized Controlled Trial to Investigate the Value of Coronary CT Angiography in the Understanding and Management of Coronary Calcium (The Optimal Trial)
The OPTIMAL randomized clinical trial has been designed to compare two imaging strategies and to test the hypothesis that a calcium modification strategy informed by coronary CT angiography (CCTA) will improve procedural efficiency and effectiveness compared with the current standard of care (IVUS-…
- Stage
- Not phased
- Ages
- 18 to 85
- Site
- Minneapolis Heart Institute, Minneapolis, Minnesota
- Locations
- 14 in total
- Run by
- Fundación EPIC
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Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery Lesions
The objective of this study is to assess the safety and efficacy of the Freesolve resorbable magnesium scaffold (RMS) in the treatment of subjects with up to two de novo lesions in native coronary arteries compared to the Xience coronary drug-eluting stent (DES) system
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- MedStar Washington Hospital Center, Washington D.C., District of Columbia
- Locations
- 3 in total
- Run by
- Teleflex
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Coronary Computed Tomography Angiography (CCTA) for the Pre-procedural Planning of Percutaneous Coronary Intervention
The CT-PLAN PCI trial will evaluate whether CCTA-guided PCI improves procedural efficiency compared with routine PCI (without pre-procedural CCTA-guidance for PCI planning) using procedural time as the primary endpoint. Key secondary outcomes will include contrast volume, radiation dose, fluoroscop…
- Stage
- Not phased
- Ages
- 22 and older
- Site
- Minneapolis Heart Institute Foundation, Minneapolis, Minnesota
- Run by
- Minneapolis Heart Institute Foundation
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Randomization of Single vs Multiple Arterial Grafts
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, …
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- University of Colorado, Boulder, Colorado
- Locations
- 59 in total
- Run by
- Weill Medical College of Cornell University
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Prospective Global Registry for the Study of Chronic Total Occlusion Intervention
Percutaneous coronary intervention (PCI) of chronic total occlusions (CTOs) is increasingly being performed in patients with advanced coronary artery disease, but there is limited information on the techniques utilized and the procedural outcomes. The goal of this multicenter, investigator initiate…
- Stage
- Not phased
- Ages
- Any age
- Site
- Little Rock VA Medical Center, Little Rock, Arkansas
- Locations
- 48 in total
- Run by
- Minneapolis Heart Institute Foundation
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Progress Complication
Coronary angiography and percutaneous coronary intervention (PCI) is often performed in patients with ischemic heart disease. The safety of PCI has improved with new devices and strategies, but complications still occur, especially during complex procedures. The objectives of this multi-center obse…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Minneapolis Heart Institute Foundation, Minneapolis, Minnesota
- Run by
- Minneapolis Heart Institute Foundation
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Progress Bifurcation Global Registry
Coronary bifurcation lesions are lesions (or blockages) that occur at or near the intersection of a major coronary artery and one of the arteries' side branches. Numerous techniques and devices have been developed to treat coronary bifurcations; however, these types of lesions remain some of the mo…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Minneapolis Heart Institute Foundation, Minneapolis, Minnesota
- Run by
- Minneapolis Heart Institute Foundation
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Late Subclinical Cardiovascular Disease in Testicular Cancer Survivors
Late subclinical cardiovascular disease in testicular cancer survivors exposed to cisplatin-based chemotherapy and bone marrow transplant
- Stage
- Not phased
- Ages
- 18 to 99
- Site
- Indiana University, Indianapolis, Indiana
- Run by
- Indiana University
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Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions
The purpose of the study is to assess the safety and efficacy of the Orsiro® Mission 48- mm Sirolimus-Eluting Coronary Stent System in the treatment of subjects with atherosclerotic lesion(s) >36 mm and ≤ 44 mm in length (by visual estimate) in the native coronary arteries with a reference vessel d…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- John Muir Medical Center, Concord, California
- Locations
- 23 in total
- Run by
- Teleflex
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Virtue® SAB in the Treatment of Coronary ISR Trial
A prospective, multi-center, single-blind, randomized (1:1), non-inferiority study comparing clinical outcomes of the Virtue® Sirolimus AngioInfusion™ Balloon (SAB) to the AGENT™ Paclitaxel Drug-Coated Balloon (DCB) in the treatment of coronary artery in-stent restenosis (ISR).
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Cardiac and Vascular Institute, Gainesville, Florida
- Locations
- 15 in total
- Run by
- Orchestra BioMed, Inc
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SELUTION 4 De Novo Small Vessel IDE Trial
Prospective, randomized controlled, single-blind, multicenter, clinical trial to demonstrate the safety and efficacy of the SELUTION SLR 014 PTCA DEB for treatment of de novo lesions in small coronary vessels, defined as reference vessel diameter (RVD) of 2.00 mm to 2.75 mm, in support of a pre-mar…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- St. Bernards, Jonesboro, Arkansas
- Locations
- 70 in total
- Run by
- M.A. Med Alliance S.A.
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Intravascular Lithotripsy With or Without Rotational Atherectomy for Coronary Calcified Nodule Treatment
The NODULE-SHOCK trial is a prospective, investigator-initiated, single-center, randomized controlled trial designed to compare the efficacy of intravascular lithotripsy (IVL) with or without rotational atherectomy (RA) in patients with coronary calcified nodules (Cohort A), and operator-determined…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mount Sinai Hospital, New York, New York
- Run by
- Annapoorna Kini
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Hybrid Group Singing
The overall objective of the planned future clinical trial is to test the investigator's central hypothesis that habitual singing over several weeks, similar to habitual exercise, will lead to sustained and favorable vascular adaptation, thereby lowering cardiovascular disease (CVD) risk. The overa…
- Stage
- Not phased
- Ages
- 55 to 89
- Site
- Medical College of Wisconsin, Milwaukee, Wisconsin
- Run by
- Medical College of Wisconsin
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ANDREAS Registry (Assessment of Novel Drug-coated Balloon Revascularization: Effectiveness, Angiographic Outcomes, and Safety)
The primary objective of this protocol is to develop a comprehensive, multicenter international prospective registry to capture long-term clinical outcomes for adult patients undergoing percutaneous coronary intervention (PCI) with drug-coated balloons (DCB) for de novo coronary artery disease.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Emory University Hospital Midtown, Atlanta, Georgia
- Locations
- 19 in total
- Run by
- Emory University
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Physiological Assessment of Severe Coronary Stenosis for Informing Planned PCI
Traditionally, the severity of a blockage (stenosis) in a coronary artery has been determined by visual angiographic assessment of the diameter of the artery at the level of a blockage compared to a normal healthy area of the same artery. With the advent of invasive physiological testing to assess …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Run by
- Beth Israel Deaconess Medical Center
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.