| Withdrawn | Impact of Cholesterol Level on Long-term Coronary Bypass Graft Patency NCT05393882 | Chinese University of Hong Kong | — |
| Not Yet Recruiting | To Evaluate the Performance and Safety of RisoR Crest Everolimus Eluting Coronary Stent System NCT07098195 | Poly Medicure Limited | N/A |
| Recruiting | Clinical Features, Current Treatment and Clinical Outcomes in Patients With INR-CAD: a Cohort Study NCT06845410 | Peking Union Medical College Hospital | — |
| Recruiting | IRIS-Coroflex NEO Cohort NCT06177743 | Seung-Jung Park | — |
| Recruiting | Diabetes-Centered Evaluation of Revascularization Strategy of Functional and Imaging-CombiNEd State-of-the-Art NCT05831085 | Duk-Woo Park, MD | N/A |
| Not Yet Recruiting | iNav-based, Automated Coronary Magnetic Resonance Angiography for the Detection of Coronary Artery Stenosis NCT05473117 | Aarhus University Hospital | — |
| Recruiting | Disease Characteristics of IR-CAD: a Case-control Study NCT06007248 | Peking Union Medical College Hospital | — |
| Unknown | Functional Diagnostic Accuracy of Ultrasonic Flow Ratio in Assessment of Coronary Artery Lesions NCT06052670 | China National Center for Cardiovascular Diseases | — |
| Completed | Anthocyanin Intake on Cardiometabolic Biomarkers NCT05995002 | Shahid Beheshti University | N/A |
| Recruiting | Efficacy and Safety of Comprehensive Treatment in Patients With IR-CAD: a Self-controlled Cohort Study NCT05860400 | Peking Union Medical College Hospital | — |
| Completed | RecoveryPlus Telerehab Platform Pilot Study NCT05804500 | NODEHealth Foundation | N/A |
| Completed | Prospective Multicenter Study to Characterize the REAL-WORLD EVIDENCE Regarding Safety and Performance of the NCT05536180 | Arthesys | — |
| Unknown | Coronary Non-slip Balloon Catheter in Patients With Coronary Artery Stenosis(CREST) NCT05606367 | Shanghai MicroPort Rhythm MedTech Co., Ltd. | N/A |
| Unknown | Study of the No-touch Saphenous Vein Graft NCT05757947 | Meshalkin Research Institute of Pathology of Circulation | N/A |
| Unknown | Effects of Mindfulness Based Therapy on Illness and Depression in Cardiac Rehab Phase-i NCT05532605 | Riphah International University | N/A |
| Completed | Compare the Effectiveness and Safety of Two Different Kinds of Cutting Balloon in Coronary Artery Disease NCT05509296 | Sino Medical Sciences Technology Inc. | N/A |
| Completed | Prospective Multicenter Study to Characterize the REAL-WORLD EVIDENCE Regarding Safety and Performance of the NCT05232565 | Arthesys | — |
| Completed | A Study to EXhibit Percutaneous Coronary Artery Dilatation With Non-Slip Element Balloon NCT04985773 | Infraredx | N/A |
| Active Not Recruiting | Sirolimus-coated Balloon Versus Drug-eluting Stent in Native Coronary Vessels - TRANSFORM II NCT04893291 | Fondazione Ricerca e Innovazione Cardiovascolare ETS | N/A |
| Recruiting | Complete Functional Assessment of Intermediate Coronary Artery Stenosis Before and After Transcatheter Aortic NCT05133843 | Helios Health Institute GmbH | N/A |
| Completed | Relation Between AI-QCA and Cardiac PET NCT06397820 | Chonnam National University Hospital | — |
| Unknown | Beta Blocker De-prescription Following Coronary Artery Bypass Graft Surgery (BEEFBURGER Trial). NCT04788186 | University of Saskatchewan | Phase 4 |
| Unknown | Evaluation on the Effectiveness and Safety of RuiXin-CoronaryAI for Diagnosis of Coronary Artery Stenosis NCT05320185 | Shenzhen Raysight Intelligent Medical Technology Co., Ltd. | — |
| Completed | A Study to Evaluate Direct Wire Pacing (DWP) for Measuring Fractional Flow Reserve (FFR) NCT04970082 | Centre Recherche Cardio Vasculaire Alpes | N/A |
| Unknown | Anatomical Assessment Versus Pull Back RFR Measurement NCT04857762 | Szabolcs - Szatmár - Bereg County Hospitals and University Teaching Hospital, András Jósa Teaching H | — |
| Active Not Recruiting | ANGiographic Evaluation of Left Main Coronary Artery INtErvention NCT04604197 | Fundación EPIC | N/A |
| Active Not Recruiting | The Elixir Bioadaptor vs. The Onyx Stent in De Novo Native Coronary Arteries NCT04192747 | Elixir Medical Corporation | N/A |
| Unknown | Optimal Predilatation Treatment Before Implantation of a Magmaris Bioresorbable Scaffold in Coronary Artery St NCT04666584 | Odense University Hospital | N/A |
| Recruiting | Vessel Imaging Using Optical Coherence Tomography for Plaque Morphology and Vessel Fractional Flow Reserve NCT06844942 | Medical University of Warsaw | — |
| Unknown | FFR and Inducible Myocardial Ischemia During Adenosine Stress Testing NCT04401657 | Asan Medical Center | N/A |
| Recruiting | Breathing-Maneuver-Induced Myocardial Oxygenation Reserve Validated by FFR (B-MORE) NCT04126148 | McGill University Health Centre/Research Institute of the McGill University Health Centre | — |
| Terminated | Use of Magnetocardiography in Evaluation of Patients Going for Cardiac Catheterization NCT04044391 | Genetesis Inc. | — |
| Completed | Functional Assessment of Myocardial Ischemia by Intracoronary Electrocardiogram NCT03985241 | Insel Gruppe AG, University Hospital Bern | N/A |
| Unknown | Optimal Predilatation Technique for BVS Implantation NCT02946320 | Cardiology Center Agel | Phase 3 |
| Unknown | Coronary Revascularization Assessed by Stress PET NCT02931331 | Ochsner Health System | — |
| Completed | Pre-market Study of the DREAMS 2G Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-III) NCT02716220 | Biotronik AG | N/A |
| Terminated | DESolve® X-Pand Global Post Market Registry NCT02453035 | Elixir Medical Corporation | — |
| Completed | Sirolimus-eluting Stent CALYPSO vs Everolimus-eluting Stent XIENCE NCT02681016 | Meshalkin Research Institute of Pathology of Circulation | N/A |
| Completed | Absorb IV Randomized Controlled Trial NCT02173379 | Abbott Medical Devices | N/A |
| Completed | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery Lesions NCT02229864 | Abbott Medical Devices | N/A |
| Completed | Angiography Study of BioNIR Drug Eluting Stent System (NIREUS) NCT01995500 | Medinol Ltd. | Phase 2 |
| Completed | Study of BioNIR Drug Eluting Stent System in Coronary Stenosis NCT01995487 | Medinol Ltd. | N/A |
| Completed | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffold NCT02066623 | IHF GmbH - Institut für Herzinfarktforschung | — |
| Unknown | First in Man Study of the DREAMS 2nd Generation Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-II) NCT01960504 | Biotronik AG | N/A |
| Completed | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) System in Chinese Population ~ NCT01923740 | Abbott Medical Devices | N/A |
| Unknown | Cordimax China Post Market Surveillance NCT03185221 | Shandong Branden Med.Device Co.,Ltd | Phase 3 |
| Completed | ReZolve2 Clinical Investigation NCT01845311 | REVA Medical, Inc. | N/A |
| Completed | Nationwide Cohort Study of Antiplatelet Agents as Primary Prevention NCT06281041 | Samsung Medical Center | — |
| Completed | ABSORB FIRST is a Registry Designed to Evaluate the Safety and Performance of Absorb Bioresorbable Vascular Sc NCT01759290 | Abbott Medical Devices | — |
| Completed | ABSORB III Randomized Controlled Trial (RCT) NCT01751906 | Abbott Medical Devices | N/A |
| Completed | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) NCT01721096 | Abbott Medical Devices | — |
| Completed | A Clinical Trials of Quick-Acting Heart Reliever for Moderate Coronary Stenosis NCT01513070 | Guang'anmen Hospital of China Academy of Chinese Medical Sciences | Phase 4 |
| Unknown | HanYang University Medical Center (HYUMC) Registry NCT05935397 | Hanyang University Seoul Hospital | — |
| Completed | Safety Study of a Bioresorbable Coronary Stent NCT01262703 | REVA Medical, Inc. | N/A |
| Withdrawn | The Real-world Firebird 2 Versus Cypher Sirolimus-eluting Stent in Treating Patients With Coronary Artery Dise NCT01328730 | Shanghai Jiao Tong University School of Medicine | Phase 4 |
| Completed | T-provisional Stenting vs Mini-Crush in Chronic Total Occlusions (CTO) NCT02708329 | Meshalkin Research Institute of Pathology of Circulation | N/A |
| Completed | Kidney Damage in Patients With Normal eGFR NCT01137786 | Bracco Diagnostics, Inc | Phase 4 |
| Terminated | Kidney Damage In Patients With Severe Fall In eGFR NCT01136915 | Bracco Diagnostics, Inc | Phase 4 |
| Completed | Kidney Damage in Patients With Moderate Fall in eGFR NCT01136876 | Bracco Diagnostics, Inc | Phase 4 |
| Completed | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval, Single-Arm Study NCT01249027 | Abbott Medical Devices | — |
| Completed | EXCEL Clinical Trial (Universal Registry) NCT01205789 | Abbott Medical Devices | — |
| Completed | Stress-MRI Assessment After Right Coronary Artery CTO Recanalization NCT02769650 | Meshalkin Research Institute of Pathology of Circulation | N/A |
| Unknown | Trial to Assess the Everolimus-Eluting Coronary Stent System (PROMUS Element) for Coronary Revascularization NCT01342822 | European Cardiovascular Research Center | — |
| Completed | EXCEL Clinical Trial NCT01205776 | Abbott Medical Devices | N/A |
| Completed | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter in Stenotic Lesions NCT01186198 | Abbott Medical Devices | — |
| Completed | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval Randomized Control Trial (RCT) NCT01178268 | Abbott Medical Devices | Phase 4 |
| Completed | Main Branch Versus Side Branch Ostial Lesion NCT01335659 | Seoul National University Hospital | — |
| Completed | Comparing the Protective Effects of Two Cardioplegic Solutions, on Cardiac Metabolism, as Assessed Using Micro NCT01401140 | Centre Hospitalier Universitaire de Saint Etienne | Phase 3 |
| Completed | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coronary Stent System in Japanese Po NCT01115933 | Abbott Medical Devices | N/A |
| Completed | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Protocol for Japan NCT01086228 | Abbott Medical Devices | — |
| Terminated | Fractional Flow Reserve (FFR) Versus Intravascular Ultrasound (IVUS) in Intermediate Coronary Artery Disease NCT01175863 | Ajou University School of Medicine | Phase 4 |
| Completed | ABSORB EXTEND Clinical Investigation NCT01023789 | Abbott Medical Devices | N/A |
| Terminated | Chronic Total Occlusion Registry NCT04041921 | Seung-Jung Park | — |
| Completed | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort NCT01106534 | Abbott Medical Devices | Phase 4 |
| Completed | De Novo Pilot Study, Lutonix Catheter in Conjunction With Bare Metal Stenting for Treatment of Coronary De Nov NCT00934752 | C. R. Bard | Phase 1 / Phase 2 |
| Completed | SPIRIT PRIME Clinical Trial NCT00916370 | Abbott Medical Devices | Phase 3 |
| Withdrawn | COmplex BifuRcation Lesions: A Comparison Between the AXXESS Device and Culotte Stenting: An Optical Coherence NCT00895791 | Universitaire Ziekenhuizen KU Leuven | N/A |
| Unknown | Comparison of Platelet Inhibition With Adjunctive Cilostazol Versus High Maintenance-Dose Clopidogrel Accordin NCT00891670 | Gyeongsang National University Hospital | Phase 3 |
| Completed | Coronary Artery Stent Evaluation With 320-slice Computed Tomography - The CArS 320 Study NCT00967876 | Charite University, Berlin, Germany | — |
| Unknown | Comparison of Fractional Flow Reserve and Intravascular Ultrasound NCT01133015 | Seoul National University Hospital | Phase 4 |
| Unknown | Fractional Flow Reserve and Intravascular Ultrasound in Evaluating Intermediate Coronary Lesions NCT01414361 | Seoul National University Hospital | — |
| Withdrawn | Steroid-induced Reduction of Surgical Stress Study NCT00807521 | Amsterdam UMC, location VUmc | N/A |
| Completed | Validation of Stenosis Assessment by Coronary Artery Computed Tomography Against Invasive Measurements of Frac NCT00817102 | Piedmont Healthcare | N/A |
| Completed | Multivessel Disease Diagnosed at the Time of PPCI for STEMI: Complete Revascularization Versus Conservative St NCT01332591 | St. Anne's University Hospital Brno, Czech Republic | N/A |
| Completed | XIENCE V: SPIRIT WOMEN Sub-study NCT01182428 | Abbott Medical Devices | Phase 4 |
| Completed | Biorest Liposomal Alendronate With Stenting sTudy (BLAST) NCT00739466 | BIOrest Ltd. | Phase 2 |
| Completed | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIENCE V® USA Long Term Follow-up NCT01120379 | Abbott Medical Devices | — |
| Completed | 320-slice Coronary Computed Tomography (CT) Angiography NCT00721851 | Charite University, Berlin, Germany | — |
| Completed | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease NCT01310309 | Abbott Medical Devices | — |
| Completed | EXecutive RCT: Evaluating XIENCE V® in a Multi Vessel Disease NCT00531011 | Abbott Medical Devices | Phase 4 |
| Terminated | Prophylactic Intra-coronary Adenosine to Prevent Post Coronary Artery Stenting Myonecrosis NCT00612521 | Ottawa Heart Institute Research Corporation | Phase 3 |
| Completed | The Effect of Pioglitazone on Neointima Volume and Inflammatory Markers NCT00494559 | Korea University Anam Hospital | Phase 4 |
| Completed | XIENCE V: SPIRIT WOMEN NCT00496938 | Abbott Medical Devices | Phase 4 |
| Completed | Healthy Endothelial Accelerated Lining Inhibits Neointimal Growth NCT00349895 | OrbusNeich | Phase 4 |
| Completed | Computed Tomographic Angiography or Conventional Coronary Angiography in Clinical Decision Making NCT00566059 | University Medical Center Groningen | — |
| Completed | SPIRIT III Clinical Trial of the XIENCE V® Everolimus Eluting Coronary Stent System (EECSS) NCT00180479 | Abbott Medical Devices | Phase 3 |
| Completed | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting Coronary Stent System NCT00180453 | Abbott Medical Devices | Phase 3 |
| Completed | Study of Unprotected Left Main Stenting Versus Bypass Surgery (LE MANS Study) NCT00375063 | Ministry of Science and Higher Education, Poland | Phase 4 |