| Not Yet Recruiting | Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With C NCT07258290 | Teleflex | N/A |
| Recruiting | Single vs. Dual Antiplatelet Therapy in Elderly or HBR Patients Undergoing Percutaneous Intervention With DCB NCT06535568 | Fondazione Ricerca e Innovazione Cardiovascolare ETS | N/A |
| Recruiting | A Prospective, Multicenter, Randomized Controlled Trial to Investigate the Value of Coronary CT Angiography in NCT07286578 | Fundación EPIC | N/A |
| Recruiting | Results of the Use of Two Stentrievers Simultaneosly Compared With One as a Primary Treatment in Acute Ischemi NCT05930145 | Fundación EPIC | N/A |
| Completed | FLEX FIRST Registry Research Protocol NCT05616104 | VentureMed Group Inc. | — |
| Unknown | Preliminary Tissue Monitoring During Endovascular Intervention Study NCT04956523 | Pedra Technology, PTE LTD | — |
| Unknown | Tissue Monitoring During Endovascular Intervention NCT04744870 | Pedra Technology, PTE LTD | — |
| Unknown | Primary FIbrinolysis and Secondary STenting Versus immEdiate Stenting in ST-segment Elevation Myocardial Infar NCT04663932 | Harbin Medical University | N/A |
| Unknown | Optimal Predilatation Treatment Before Implantation of a Magmaris Bioresorbable Scaffold in Coronary Artery St NCT04666584 | Odense University Hospital | N/A |
| Completed | Clinical Trial to Evaluate the Efficacy and Safety of Sarpogrelate SR in Patients With Chronic Artery Occlusiv NCT06046196 | Yuhan Corporation | Phase 4 |
| Completed | Dual Anti-Platelet Therapy in Patients With Coronary Multi-Vessel Disease (DAPT-MVD) NCT04624854 | Harbin Medical University | Phase 4 |
| Active Not Recruiting | Multivessel TALENT NCT04390672 | National University of Ireland, Galway, Ireland | N/A |
| Completed | Ammonia N-13 Myocardial Blood Flow Absolute Quantification by PET in Patients With Known or Suspected CAD (Amm NCT04343209 | Ionetix Corporation | — |
| Unknown | Safety and Feasibility Evaluation of Planning and Execution of Surgical Revascularization Solely Based on Coro NCT04142021 | National University of Ireland, Galway, Ireland | — |
| Completed | Registry of Coronary Lithotripsy in Spain. NCT04298307 | Fundación EPIC | — |
| Unknown | PROMISE II: Percutaneous Deep Vein Arterialization for the Treatment of Late-Stage Chronic Limb-Threatening Is NCT03970538 | LimFlow, Inc. | N/A |
| Unknown | LegDeb2 Global Registry for Use of Legflow in Peripheral Arteries NCT04175197 | Federico II University | — |
| Completed | The Role of microRNA-210 in Regulating Oxidative Stress in Patients With PAD NCT04089943 | University of West Florida | N/A |
| Unknown | Intracranial Stenting in Non-acute Symptomatic Ischemic Stroke NCT05063630 | Can Tho Stroke International Services Hospital | N/A |
| Completed | Distributed Registry NCT03898570 | Stanford University | — |
| Recruiting | Spectroscopy in Functional Assessment of Peripheral Artery Disease (spectroAMI) NCT03723473 | Centre Hospitalier Universitaire de Saint Etienne | — |
| Completed | Crossing Atheroma or Thrombus With ByCross Device for Revascularization of Peripheral Arteries of Diameter ≥ 3 NCT03724279 | Taryag Medical Ltd. | N/A |
| Completed | Telephone Health Coaching and Remote Exercise Monitoring for Peripheral Artery Disease NCT03496948 | Universitätsklinikum Hamburg-Eppendorf | N/A |
| Completed | Real World Registry Assessing the Clinical Use of the Bard UltraScore Forced Focus PTA Balloon NCT03193619 | C. R. Bard | — |
| Completed | The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia NCT03856606 | University of Texas at Austin | N/A |
| Completed | Prospective Multicenter Registry On Radiation Dose Estimates Of Cardiac CT Angiography in Daily Practice in 20 NCT03253692 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Completed | Functional Diagnostic Accuracy of Quantitative Flow Ratio in Tandem Lesions and Virtual Stenting NCT03405506 | Pulse Medical Imaging Technology (Shanghai) Co., Ltd | — |
| Completed | The FAVOR II China Study NCT03191708 | China National Center for Cardiovascular Diseases | — |
| Completed | A Real World Evaluation of the ELUVIA Stent in Subjects With Lesions Located in the Femoropopliteal Arteries NCT03037411 | Boston Scientific Corporation | — |
| Completed | Trial Comparing ELUVIA Versus Bare Metal Stent in Treatment of Superficial Femoral and/or Proximal Popliteal A NCT02921230 | Boston Scientific Corporation | N/A |
| Unknown | Ischemic Pain Control With Analgesic Methods Clinical Trial NCT02841488 | University of Sao Paulo General Hospital | Phase 3 |
| Unknown | A Prospective Study: the Value of Using iFlow and PBV in the Endovascular Treatment of Infrapopliteal Arterial NCT03248323 | Peking Union Medical College Hospital | — |
| Terminated | IRIS-BVS AMI Registry NCT02699671 | Duk-Woo Park, MD | — |
| Completed | Safety of PZ-128 in Subjects Undergoing Non-Emergent Percutaneous Coronary Intervention NCT02561000 | Tufts Medical Center | Phase 2 |
| Unknown | Late Stent Strut Apposition and Coverage After Drug-Eluting Stent Implantation by OCT in Patients With AMI NCT02770651 | Keimyung University Dongsan Medical Center | — |
| Terminated | Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice NCT02622100 | Duk-Woo Park, MD | — |
| Active Not Recruiting | IRIS-Onyx Cohort in the IRIS-DES Registry NCT02593994 | Seung-Jung Park | — |
| Completed | The Transfusion Triggers in Vascular Surgery Trial NCT02465125 | Naestved Hospital | Phase 2 |
| Completed | Safety/Tolerability and Pharmacokinetic Study of SID142 NCT02625714 | SK Chemicals Co., Ltd. | Phase 1 |
| Terminated | The ABSORB Bioresorbable Scaffold Below the Knee (BTK) Study NCT02793349 | The University of New South Wales | N/A |
| Completed | Real-World Registry Assessing the Clinical Use of the Lutonix 035 Drug Coated Balloon Catheter NCT02424383 | C. R. Bard | N/A |
| Completed | The COPPER-B Trial NCT02395744 | Horizons International Peripheral Group | N/A |
| Completed | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Superficial Femoral Artery NCT02212470 | Instituto Dante Pazzanese de Cardiologia | Phase 4 |
| Withdrawn | Telerobotic Ultrasound for Carotid Imaging - Feasibility Study NCT05654935 | Rush University Medical Center | — |
| Completed | EXCEL-II Stent Vesus EXCEL Stent to Treat the Patients With de Novo Coronary Artery Lesions. NCT02057978 | JW Medical Systems Ltd | — |
| Completed | Clinical Benefits of B-Flow Ultrasound NCT02008097 | University of Washington | N/A |
| Unknown | The ASSURE ROT Registry: Bioresorbable Vascular Scaffold Following Rotablation for Complex Coronary Lesions NCT01915420 | Medical Care Center Prof. Mathey, Prof. Schofer, Ltd. | — |
| Completed | Post-Market CorPath Registry on the CorPath 200 System in Percutaneous Coronary Interventions NCT01917682 | Corindus Inc. | — |
| Completed | Neurological Complications Comparing Endoscopically vs. Open Harvest of the Radial Artery NCT01848886 | Rigshospitalet, Denmark | N/A |
| Completed | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting Bioresorbable Vascular Scaffold NCT01583608 | Medical Care Center Prof. Mathey, Prof. Schofer, Ltd. | — |
| Terminated | The eSVS® Mesh Post-Marketing Trial NCT01520311 | Kips Bay Medical, Inc. | N/A |
| Terminated | The eSVS® Mesh Randomized Post-Market Study NCT01462721 | Kips Bay Medical, Inc. | N/A |
| Completed | GORE Flow Reversal System and GORE Embolic Filter Extension Study NCT01343667 | W.L.Gore & Associates | N/A |
| Completed | Evaluation of the Safety and Effectiveness of the CorPath 200 System in Percutaneous Coronary Interventions (P NCT01275092 | Corindus Inc. | Phase 2 |
| Unknown | The Use of Cardiovascular Biomarkers in Abdominal Aortic Surgery NCT02122497 | Prim PD Dr Afshin Assadian | — |
| Completed | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatment of De Novo Lesions in Small D NCT01150500 | Medtronic Vascular | N/A |
| Unknown | Comparison of Stent and Prothesis Bypass in Superficial Femoral Artery NCT01147419 | Peking Union Medical College Hospital | Phase 4 |
| Completed | Combined Non-invasive Coronary Angiography and Myocardial Perfusion Imaging Using 320 Detector Computed Tomogr NCT00934037 | Johns Hopkins University | Phase 3 |
| Completed | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary Stent NCT00927940 | Medtronic Vascular | N/A |
| Completed | Feasability Study of Autologous Bone Marrow Aspirate Concentrate for Treatment of CLI NCT00595257 | Harvest Technologies | Phase 1 / Phase 2 |
| Completed | A Dose Escalation and Safety Study of Plasmin (Human) In Acute Lower Extremity Native Artery or Bypass Graft O NCT00418483 | Grifols Therapeutics LLC | Phase 1 |
| Completed | Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI) NCT00371371 | UMC Utrecht | Phase 1 / Phase 2 |
| Terminated | Study of Alfimeprase's Ability to Dissolve Blood Clots in the Leg and Help Prevent the Need for Surgery NCT00338585 | ARCA Biopharma, Inc. | Phase 3 |
| Completed | YUKON-drug-eluting Stent Below The Knee - Randomised Double-blind Study NCT00664963 | Herz-Zentrums Bad Krozingen | Phase 4 |
| Terminated | The Study to Compare the Treatment of Angioplasty and Stents in SFA Occlusions. NCT00289055 | Cordis US Corp. | Phase 4 |
| Completed | Safety and Feasibility Study of Autologous Bone Marrow Cell Transplantation in Patients With Peripheral Arteri NCT00282646 | Johann Wolfgang Goethe University Hospital | Phase 2 |
| Completed | The Study to Compare the Cordis SMART™ Stent System With the Bard® Luminexx™ Stent NCT00235131 | Cordis US Corp. | Phase 4 |
| Completed | Study of Alfimeprase to Rapidly Dissolve Blood Clots in the Leg and Help Prevent the Need for Surgery on Leg A NCT00115999 | ARCA Biopharma, Inc. | Phase 3 |
| Terminated | Intra-arterial Microplasmin Administration in Patients With Acute Peripheral Arterial Occlusion NCT00123292 | ThromboGenics | Phase 2 |
| Completed | The Study to Treat Superficial Femoral Artery Occlusions. NCT00232843 | Cordis US Corp. | Phase 4 |
| Completed | A Safety and Efficacy Clinical Study to Evaluate the Narrowing of the Aorto-iliac Arteries While Using Gadodia NCT00209443 | GE Healthcare | Phase 3 |
| Completed | CASPAR : Clopidogrel and Acetyl Salicylic Acid in Bypass Surgery for Peripheral ARterial Disease NCT00174759 | Sanofi | Phase 3 |
| Unknown | Thunder Trial - Local Taxan With Short Time Contact for Reduction of Restenosis in Distal Arteries NCT00156624 | University Hospital Tuebingen | Phase 2 / Phase 3 |
| Completed | High Dose Candesartan Versus Quinapril for Restenosis Prophylaxis After Stent Angioplasty NCT00154050 | Technische Universität Dresden | N/A |
| Completed | The ENDEAVOR II Clinical Trial: The Medtronic Endeavor Drug Eluting Coronary Stent System in Coronary Artery L NCT00614848 | Medtronic Vascular | N/A |
| Completed | Alfimeprase for Thrombolysis in Acute Peripheral Arterial Occlusion NCT00073554 | ARCA Biopharma, Inc. | Phase 2 |
| Completed | Best Revascularisation Approach for Posterior Circulation Strokes With Isolated Vertebral Artery Occlusions NCT05503212 | Centre Hospitalier Universitaire Vaudois | — |
| Terminated | SIMPADICO - Study of Immune Modulation Therapy in Peripheral Arterial Disease and Intermittent Claudication Ou NCT00111826 | Vasogen | Phase 3 |
| Completed | Mechanisms of Disability in Peripheral Arterial Disease NCT00046592 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Unknown | Rio Trial - ReoPro and Peripheral Arterial Intervention to Improve Clinical Outcome in Patients With Periphera NCT00156611 | University Hospital Tuebingen | Phase 2 / Phase 3 |
| Completed | Prevention of Autogenous Vein Graft Failure in Peripheral Artery Bypass Procedures NCT00041925 | Anesiva, Inc. | Phase 2 / Phase 3 |
| Completed | Blood Factors and Peripheral Arterial Disease Outcomes NCT00035776 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Completed | Plasma Transfusion in Major Vascular Surgery NCT04514575 | Naestved Hospital | — |
| Completed | Potential Role of CMV in Restenosis Following Angioplasty, in Atherosclerosis, and in Endothelial Dysfunction NCT00001531 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Completed | Dacron vs Dardik for Fem-Pop Bypass NCT00523263 | Radboud University Medical Center | Phase 3 |
| Completed | Arterial Disease Multifactorial Intervention Trial (ADMIT) NCT00000539 | National Heart, Lung, and Blood Institute (NHLBI) | Phase 3 |
| Completed | Natural History of Peripheral Arterial Disease NCT00005254 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Completed | Cholesterol-Lowering Atherosclerosis Study (CLAS) NCT00000599 | National Heart, Lung, and Blood Institute (NHLBI) | Phase 3 |
| Completed | Etiology and Prevalence of Peripheral Arterial Disease NCT00005142 | National Heart, Lung, and Blood Institute (NHLBI) | — |
| Completed | Framingham Heart Study NCT00005121 | National Heart, Lung, and Blood Institute (NHLBI) | — |