| Recruiting | EVERO Drug-coated Balloon (DCB) Randomized Trial NCT07144150 | Cook Research Incorporated | N/A |
| Recruiting | Observing the Role of Inflammation in Peripheral Artery Disease and Its Impact on Heart and Mobility Health: P NCT07500610 | Cardiology Research UBC | — |
| Recruiting | Improving Mobility After Revascularization in Peripheral Artery Disease NCT06686121 | Northwestern University | Phase 3 |
| Not Yet Recruiting | Mobility Assessment in Multi-morbidity NCT06473168 | Northumbria University | — |
| Not Yet Recruiting | Colonoscopy and Antiplatelet Therapy Trial NCT06613191 | Ochsner Health System | Phase 4 |
| Recruiting | Leg Exercise Assistive Paddling (LEAP) Therapy for Peripheral Artery Disease NCT06389149 | University of Nebraska | N/A |
| Recruiting | ENhancing Exercise With LIGHT to Improve Functioning in PAD NCT06399900 | Northwestern University | N/A |
| Recruiting | Treatment of TASC C and D Aortoiliac Lesions NCT06253312 | Clinical Centre of Serbia | — |
| Recruiting | Far Red Light to Improve Functioning in PAD NCT06165016 | Northwestern University | N/A |
| Unknown | Evaluation of an Electronic Health Record-based Screening Tool for Peripheral Artery Disease NCT04054232 | Stanford University | N/A |
| Completed | Impedance Sensor Evaluated in Peripheral Artery Disease for Tissue Detection NCT06112054 | Sensome | N/A |
| Completed | Guided Meditation to Decrease Perioperative Anxiety and Increase Patient Intraoperative Compliance in Vascular NCT05837481 | Massachusetts General Hospital | N/A |
| Completed | Effect of Plasma Ceramides on Peripheral Vascular Function NCT05107869 | Medical College of Wisconsin | N/A |
| Unknown | Post-market Clinical Investigation of the Angio-Seal™ VIP VCD (ANGIO-SEAL CLOSE) NCT05335525 | Terumo Europe N.V. | — |
| Completed | BOLT Lithotripsy RESTORE BTK Trial NCT05535907 | Bolt Medical | N/A |
| Completed | The Effect of Ischemic Conditioning on Strength and Ambulation in Subjects with PAD NCT04937179 | University of Illinois at Chicago | N/A |
| Completed | Post-Market Clinical Investigation of the FemoSeal™ VCS: A Prospective, Multi-Center Observational European St NCT05027698 | Terumo Europe N.V. | — |
| Active Not Recruiting | Does Increasing Oxygen Nurture Your Symptomatic Ischemic Ulcer Sufficiently? NCT05804097 | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | Phase 4 |
| Completed | Project to Improve Communication About Serious Illness--Hospital Study: Comparative Effectiveness Trial (Trial NCT04283994 | University of Washington | N/A |
| Terminated | Safety and Efficacy of the URECA CTO Device NCT04385381 | Ureca BV | N/A |
| Completed | Muscle Perfusion in Patients With PAD by Non-invasive MSOT NCT04641091 | University Hospital Erlangen | — |
| Unknown | Topical Gentamicin and Vancomycin for Vascular Surgical Site Infection Prophylaxis NCT04238923 | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's | Phase 2 / Phase 3 |
| Completed | Project to Improve Communication About Serious Illness--Hospital Study: Pragmatic Trial (Trial 1) NCT04281784 | University of Washington | N/A |
| Completed | Preoperative Continuous Sciatic Perineural Analgesia in Patients Undergoing Lower Limb Revascularization NCT04286971 | Hospital Municipal Miguel Couto | — |
| Withdrawn | Blood Flow Changes in Femoral-popliteal Bypass Grafts After Neuromuscular Electrical Stimulation (NMES). NCT04109287 | Imperial College Healthcare NHS Trust | N/A |
| Unknown | PROMISE II: Percutaneous Deep Vein Arterialization for the Treatment of Late-Stage Chronic Limb-Threatening Is NCT03970538 | LimFlow, Inc. | N/A |
| Completed | Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia (NL003-CLI-III-2) NCT04274049 | Beijing Northland Biotech. Co., Ltd. | Phase 3 |
| Terminated | Intermittent Negative Pressure; Impact on Peripheral Artery Disease and Intermittent Claudication NCT04100681 | Otivio AS | N/A |
| Terminated | The Value of Screening for HPR in Patients Undergoing Lower Extremity Arterial Endovascular Interventions NCT04007055 | Marissa Jarosinski | Phase 3 |
| Completed | Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia (NL003-CLI-III-1) NCT04275323 | Beijing Northland Biotech. Co., Ltd. | Phase 3 |
| Unknown | The VaSecure BTK Study NCT03638115 | Vascuros Medical Pte Ltd | N/A |
| Completed | Project to Improve Communication About Serious Illness - Pilot Study NCT03746392 | University of Washington | N/A |
| Completed | Ischemic Preconditioning Claudication Study NCT03511157 | Medical College of Wisconsin | N/A |
| Completed | JET-RANGER Trial - JETStream Atherectomy With Adjunctive Paclitaxel-Coated Balloon Angioplasty vs Plain Old Ba NCT03206762 | Midwest Cardiovascular Research Foundation | N/A |
| Unknown | Autologous Transplantation of BM-ECs With Platelet-Rich Plasma Extract for the Treatment of Critical Limb Isch NCT02993809 | South China Research Center for Stem Cell and Regenerative Medicine | Phase 1 |
| Unknown | Motivating Structured Walking Activity in Intermittent Claudication NCT03238222 | Guy's and St Thomas' NHS Foundation Trust | N/A |
| Completed | Safety and Efficacy of the SurVeil™ Drug-Coated Balloon NCT03241459 | SurModics, Inc. | N/A |
| Completed | A Clinical and Histological Analysis of Mesenchymal Stem Cells in Amputation NCT02685098 | Indiana University | Phase 1 |
| Completed | VQI DELTA Paclitaxel Device Safety Analysis NCT04110288 | Lahey Clinic | — |
| Unknown | Absorbable Sutures in Vascular Surgery NCT02935127 | University of Catanzaro | N/A |
| Completed | The DESappear Study: Drug Eluting Scaffold NCT02869087 | Elixir Medical Corporation | N/A |
| Unknown | Determining Predictors of Restenosis in Femoropopliteal Lesions NCT02734095 | University of Campinas, Brazil | N/A |
| Completed | Study of Safety and Tolerability of UNIFUZOL (Solution for Infusions) in Healthy Volunteers NCT03028285 | POLYSAN Scientific & Technological Pharmaceutical Company | Phase 1 |
| Terminated | Prehabilitation for PAD Revascularization Patients NCT02767895 | University of Michigan | N/A |
| Completed | Tele-Health Electronic Monitoring to Reduce Post Discharge Complications and Surgical Site Infections NCT02767011 | CAMC Health System | N/A |
| Completed | BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease NCT02655887 | C. R. Bard | N/A |
| Active Not Recruiting | BGC101 (EnEPC) Autologous Cell Therapy From Patient's Own Blood for Treatment of Critical Limb Ischemia (CLI) NCT02805023 | BioGenCell Ltd. | Phase 1 / Phase 2 |
| Completed | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed FemoropopliTeal ArterY Lesions NCT02850107 | VIVA Physicians | N/A |
| Completed | Ultrasound-guided Femoral Vein Accessibility, Safety and Time for Atrial Fibrillation Treatment NCT02834221 | Kenichiro Yamagata | N/A |
| Completed | Vorapaxar on Thrombin Generation and Coagulability NCT03207451 | Inova Health Care Services | Phase 4 |
| Unknown | Umbilical Cord Mesenchymal Stem Cells Infusion for Diabetes Related Vascular Complications NCT02834858 | Jie Shen | Phase 1 |
| Terminated | Oral Nutritional Supplement in Reducing Surgical Site Infections NCT02475525 | University of Limerick | N/A |
| Completed | The OPC for Optimal Delivery of Paclitaxel for the Prevention of Endovascular Restenosis - Above and Below the NCT02464501 | Horizons International Peripheral Group | N/A |
| Active Not Recruiting | Shockwave Therapy in Lower Limb Intermittent Calf Claudication NCT02652078 | Hull University Teaching Hospitals NHS Trust | N/A |
| Completed | A Study on the Use of CorMatrix® ECM® for Femoral Arterial Reconstruction NCT02418156 | Elutia Inc. | — |
| Completed | The COPPER-B Trial NCT02395744 | Horizons International Peripheral Group | N/A |
| Unknown | A Clinical Study Using Autologous Bone Marrow Stem Cell for Diabetes Related Vascular Complications NCT02796079 | Jie Shen | Phase 1 |
| Unknown | A Clinical Study Using Adipose-derived Stem Cells for Diabetic Foot NCT02831075 | Jie Shen | Phase 1 |
| Completed | Atherectomy By Laser Ablation With Turbo-Elite NCT02307370 | Spectranetics Corporation | N/A |
| Completed | Neuromuscular Electrical Stimulation (NMES) in Patients With Intermittent Claudication NCT02436200 | Imperial College London | N/A |
| Completed | Adjuvant Benefit of NMES to Supervised Exercise in Patients With IC NCT02429310 | Imperial College London | N/A |
| Terminated | Exparel as a Nerve Block for Severe Hand Pain NCT02374320 | Jose Soberon, MD | Phase 2 / Phase 3 |
| Completed | Zilver PTX Delivery System NCT02271529 | Cook Group Incorporated | N/A |
| Completed | BARD® Study of LIFESTREAM™ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease NCT02228564 | C. R. Bard | N/A |
| Unknown | Safety and Efficacy of Autologous Bone Marrow Stem Cells for Lower Extremity Ischemia Treating NCT01903044 | Pontifícia Universidade Católica do Paraná | Phase 1 / Phase 2 |
| Completed | Prospective, Non-randomized Multi-center, Controlled Physician-initiated Trial: Rotarex Belgium In-stent Occlu NCT02212626 | Flanders Medical Research Program | Phase 4 |
| Unknown | The Cook Zilver PTX Drug-eluting Stent Versus Bypass Surgery for the Treatment The Cook Zilver PTX Drug-elutin NCT01952457 | Flanders Medical Research Program | Phase 4 |
| Completed | Physician-Initiated Trial Investigating the BeGraft Peripheral Stent Graft System NCT02211716 | Flanders Medical Research Program | Phase 4 |
| Completed | Physician-Initiated Trial Investigating the Efficacy of Endovascular Treatment of Femoropopliteal Arterial Ste NCT02211664 | Flanders Medical Research Program | Phase 4 |
| Completed | Luminor Registry: Registry of the Results of Angioplasty With Drug-eluting Balloon (Paclitaxel) in the Treatme NCT02458911 | iVascular S.L.U. | — |
| Terminated | Embolization Procedures in the Peripheral Vasculature Using the Magellan™ Robotic System NCT02369692 | Hansen Medical | — |
| Completed | Pilot Safety Study of Injectable SIS for Critical Limb Ischemia NCT02145845 | Cook Group Incorporated | N/A |
| Withdrawn | Telerobotic Ultrasound for Carotid Imaging - Feasibility Study NCT05654935 | Rush University Medical Center | — |
| Completed | Drug-Coated Chocolate PTA Balloon in Patients With Peripheral Arterial Disease - The ENDURE Trial NCT02129127 | TriReme Medical, LLC | N/A |
| Completed | The Effect of Heat on Blood and Oxygen Flow Readings Part 2 NCT01992939 | VA Pittsburgh Healthcare System | N/A |
| Terminated | Registry of the Magellan Robotic System NCT01984437 | Hansen Medical | — |
| Completed | Evaluation of the Safety and Efficacy of a Vascular Prosthesis as an Above-Knee Bypass Graft in Patients With NCT01872208 | Humacyte, Inc. | N/A |
| Unknown | RCT to Evaluate the Renal Protective Effects of Remote Ischaemic Preconditioning in Peripheral Angioplasty NCT02054871 | Mid Western Regional Hospital, Ireland | N/A |
| Completed | Effect of Nike FuelBand on Exercise and Function in Claudicants; a Randomised Controlled Trial NCT01822457 | Imperial College London | N/A |
| Completed | Platelet Activity in Vascular Surgery for Thrombosis and Bleeding NCT01897103 | NYU Langone Health | — |
| Withdrawn | Lower Extremity Regional Anesthesia and Infrainguinal Bypass Grafting NCT01803165 | University of Nebraska | — |
| Unknown | Effects of Prevena Therapy on Obese and or Diabetic Patients With Surgical Groin Sites NCT01983215 | Dr. Jean E. Starr, MD | N/A |
| Completed | Pilot Study to Determine Percent Tissue Perfusion and Cellular Viability Using SPY Imaging NCT01522495 | Georgetown University | N/A |
| Completed | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" NCT02786173 | Metro Health, Michigan | — |
| Completed | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal NCT01938391 | Abbott Medical Devices | N/A |
| Withdrawn | Popliteal Artery of Treatment With Balloon Angioplasty vs. SUPERA VERITAS Peripheral Stent System NCT01667393 | Abbott Medical Devices | N/A |
| Completed | Lowering the Risk of Operative Complications Using Atorvastatin Loading Dose NCT01543555 | Hospital do Coracao | Phase 3 |
| Completed | Open-label Pilot Study to Assess the Use of Magic Foot™ in the Improvment of Parameters in Subject With Foot S NCT01784471 | Yaffa Golan, Ltd. | N/A |
| Unknown | Study to Determine the Performance of the Astron and Pulsar-18 Stents in Europe NCT01661231 | Biotronik AG | N/A |
| Completed | JetStream (JS) Atherectomy in Femoropopliteal In-Stent Restenotic Lesions NCT01722877 | Midwest Cardiovascular Research Foundation | N/A |
| Completed | Tack Optimized Balloon Angioplasty (TOBA) Study NCT01663818 | Philips Clinical & Medical Affairs Global | N/A |
| Completed | Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia NCT01548378 | Beijing Northland Biotech. Co., Ltd. | Phase 2 |
| Completed | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbable Vascular Scaffold) System NCT01468974 | Abbott Medical Devices | N/A |
| Terminated | The ABSORB BTK (Below The Knee) Clinical Investigation NCT01341340 | Abbott Medical Devices | N/A |
| Completed | Absolute Pro® MOMENTUM™ NCT01444378 | Abbott Medical Devices | N/A |
| Completed | Evaluation of Safety and Efficacy of the FlexStent® Femoropopliteal Self-Expanding Stent System NCT01355406 | Cordis US Corp. | N/A |
| Completed | Near Infrared Spectroscopy and Transcutaneous Oxygen Pressure in Critical Limb Ischemia Before and After Treat NCT01459341 | Carmel Medical Center | — |
| Completed | Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents NCT01319812 | Biotronik, Inc. | Phase 2 |
| Completed | Effects of Paclitaxel on Intimal Hyperplasia NCT01454778 | Patrick Kelly | N/A |
| Completed | PF-00489791 For The Treatment Of Raynaud's NCT01090492 | Pfizer | Phase 2 |
| Completed | Endovascular Atherectomy Safety and Effectiveness Study NCT01541774 | AtheroMed, Inc | Phase 3 |
| Completed | A Multi-center Clinical Trial of the Misago™ Self-Expanding Stent System for Superficial Femoral Artery NCT01118117 | Terumo Medical Corporation | N/A |
| Completed | 4-EVER : a Trial Investigating the Safety of 4F Endovascular Treatment of Infra-Inguinal Arterial Stenotic Dis NCT01413139 | Flanders Medical Research Program | Phase 4 |
| Completed | Atrial Fibrillation Registry for Ankle-brachial Index Prevalence Assessment: Collaborative Italian Study. NCT01161251 | University of Roma La Sapienza | — |
| Completed | Bard® LifeStent® Vascular Stent Delivery System Study NCT01179984 | C. R. Bard | N/A |
| Terminated | Safety and Efficacy Study of Autologous Concentrated Bone Marrow Aspirate (cBMA) for Critical Limb Ischemia (C NCT01049919 | Zimmer Biomet | N/A |
| Completed | The Evicel Post-Authorization Surveillance Study NCT01158261 | Ethicon, Inc. | — |
| Completed | GORE VIABAHN® Versus Plain Old Balloon Angioplasty (POBA) for Superficial Femoral Artery (SFA) In-Stent Resten NCT01108861 | Flanders Medical Research Program | Phase 4 |
| Completed | Study to Compare 2 Doses of Polycap Versus Single Dose of Polycap With or Without Pottasium NCT01404078 | St. John's Research Institute | N/A |
| Terminated | Clinical Pilot-Study of ProEndoTecc Vascular Grafts as Superficial Femoral Artery Bypass / Interponate NCT01095237 | NonWoTecc Medical GmbH | N/A |
| Unknown | Paclitaxel Eluting Balloon and Conventional Balloon for In-Stent Restenosis of the Superficial Femoral Artery NCT01083394 | Deutsches Herzzentrum Muenchen | Phase 4 |
| Active Not Recruiting | Safety Study of MultiGeneAngio in Patients With Chronic Critical Limb Ischemia NCT00956332 | MultiGene Vascular Systems Ltd. | Phase 1 / Phase 2 |
| Completed | Physical Activity, Function and Quality of Life in Patients After Endovascular Treatment NCT01109732 | Oslo University Hospital | N/A |
| Completed | TomVasc - Vascular Effects of Tomato Extract NCT01100385 | Cambridge University Hospitals NHS Foundation Trust | N/A |
| Completed | Registry of AngioJet Use in the Peripheral Vascular System NCT01086215 | Boston Scientific Corporation | — |
| Completed | Standard Balloon Angioplasty Versus Angioplasty With a Paclitaxel-eluting Balloon for Femoral Artery In-stent NCT01305070 | Medical Care Center Prof. Mathey, Prof. Schofer, Ltd. | Phase 4 |
| Completed | Safety of Intramuscular Injections (IM) of Allogeneic PLX-PAD Cells for the Treatment of Critical Limb Ischemi NCT00951210 | Pluristem Ltd. | Phase 1 |
| Completed | Comparison of the SUpera® PERipheral System in the Superficial Femoral Artery NCT00933270 | Abbott Medical Devices | N/A |
| Unknown | VKORC1 and CYP2C9 Gene Polymorphisms and Warfarin Management NCT00970892 | Ankara University | — |
| Completed | Safety of Intramuscular Injection of Allogeneic PLX-PAD Cells for the Treatment of Critical Limb Ischemia NCT00919958 | Pluristem Ltd. | Phase 1 |
| Completed | A Study to Collect Intravascular Ultrasound Images Before and After Treatment With the Jetstream System NCT00911417 | Pathway Medical Technologies Inc. | Phase 4 |
| Unknown | SAMBA EU Femoropopliteal Trial NCT01139177 | NovoStent Corporation | N/A |
| Completed | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System in Subject NCT00844532 | Abbott Medical Devices | Phase 3 |
| Completed | Trial to Evaluate the Safety & Efficacy of the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in S NCT01396525 | Abbott Medical Devices | Phase 3 |
| Terminated | Normalization of Fasting Glucose and the Incidence of Restenosis After Peripheral Angioplasty NCT01150617 | IRCCS San Raffaele | Phase 4 |
| Completed | Efficacy Study of Iliac Stents to Treat TASC A-B-C-D Iliac Artery Lesions NCT00764777 | Flanders Medical Research Program | Phase 4 |
| Completed | The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions NCT00814970 | Medtronic Endovascular | N/A |
| Completed | Study Comparing Two Methods of Expanding Stents Placed in Legs of Diabetics With Peripheral Vascular Disease NCT00827853 | North Texas Veterans Healthcare System | N/A |
| Terminated | Data Registry Following Patients Using Supera Stent in the Femoral Arteries NCT01154751 | Abbott Medical Devices | N/A |
| Completed | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study NCT00753337 | Medtronic Endovascular | N/A |
| Completed | Evaluation of Cilostazol in Combination With L-Carnitine NCT00822172 | Colorado Prevention Center | Phase 4 |
| Completed | Placement of Peripherally Inserted Central Venous Catheters (PICC) in Children Guided by Ultrasound NCT01279642 | Federal University of São Paulo | N/A |
| Completed | Angio-Seal Evolution Device Registry NCT00817349 | Abbott Medical Devices | — |
| Completed | Phase II Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia NCT00721006 | TCA Cellular Therapy | Phase 2 |
| Completed | Non-Contrast Enhanced Peripheral Magnetic Resonance Angiography NCT02823444 | University of Utah | — |
| Completed | Femoral Arterial Access With Ultrasound Trial NCT00667381 | University of California, Irvine | N/A |
| Completed | Drug Eluting Stents In The Critically Ischemic Lower Leg NCT00510393 | Flanders Medical Research Program | Phase 2 |
| Completed | DURABILITY-200: EverFlex 200mm Long Nitinol Stents in TASC C&D Femoropopliteal Lesions NCT00637741 | Flanders Medical Research Program | Phase 4 |
| Completed | Injection of Autologous CD34-Positive Cells for Critical Limb Ischemia NCT00616980 | Losordo, Douglas, M.D. | Phase 1 / Phase 2 |
| Completed | The Complete® Self-Expanding Stent and Stent Delivery System Registry NCT00730730 | Medtronic Endovascular | N/A |
| Completed | Evaluation of the Effect of the Flowaid Device in Increasing Local Circulation in the Leg NCT00538226 | Rosenblum, Jonathan I., DPM | Phase 1 |
| Completed | Atrium iCAST Iliac Stent Pivotal Study NCT00593385 | Atrium Medical Corporation | N/A |
| Withdrawn | Radiofrequency for the Treatment of Peripheral Vascular Occlusive Disease of the Lower Extremities NCT00751283 | Vessix Vascular, Inc | Phase 2 / Phase 3 |
| Terminated | Multicenter Assessment of the Safety and Efficacy of the Minnow Medical GRST™ Peripheral Catheter System NCT00881257 | Vessix Vascular, Inc | Phase 2 / Phase 3 |
| Unknown | PTA and Drug Eluting Stents for Infrapopliteal Lesions in Critical Limb Ischemia NCT00471289 | Netherlands Society for Interventional Radiology | Phase 2 / Phase 3 |
| Completed | Belgian Prospective Multicentre Registry on the Performance of the Smart Stent in the Superficial Femoral Arte NCT00496041 | University Hospital, Ghent | N/A |
| Completed | Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia NCT00518401 | TCA Cellular Therapy | Phase 1 |
| Unknown | Evaluation of the Clinical Significance of Fluorescence Videoangiography With Indocyanine-Green NCT00876668 | Johann Wolfgang Goethe University Hospital | — |
| Completed | Study of the SafeSeal(TM) Hemostasis Patch Following Percutaneous Coronary Artery and Peripheral Vascular Inte NCT00481741 | University of Rochester | Phase 4 |
| Completed | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral Stent System NCT00475566 | Abbott Medical Devices | N/A |
| Unknown | Autologous Bone Marrow Stem Cell Transplantation for Critical, Limb-threatening Ischemia NCT00434616 | Franziskus-Krankenhaus | Phase 2 / Phase 3 |
| Terminated | Study to Evaluate Safety & Effectiveness of Vascular Sealant System NCT00439309 | Integra LifeSciences Corporation | N/A |
| Terminated | FIRE-PAD: Functional Improvement Through Revascularization of the Extremities for Peripheral Arterial Disease NCT00274157 | The Cleveland Clinic | — |
| Completed | Effects of Cilostazol on VEGF and Oxidative Stress Biomarkers in Hemodialysis Patients With Peripheral Vascula NCT00431249 | Tungs' Taichung Metroharbour Hospital | Phase 4 |
| Unknown | A Prospective Study to Assess the Screening Value of N-terminal Pro-B-type Natriuretic Peptide (NT-proBNP) for NCT00519961 | Hoffmann-La Roche | N/A |
| Completed | Crossover Study With MultiHance vs a Comparator for Peripheral MRA NCT00408083 | Bracco Diagnostics, Inc | Phase 3 |
| Unknown | RESTORE-IT-Study of Rifalazil in Chlamydia Pneumoniae Seropositive Patients With a History of Atherosclerotic NCT00385385 | ActivBiotics | Phase 2 |
| Completed | ALD-301 for Critical Limb Ischemia, Randomized Trial NCT00392509 | Aldagen | Phase 1 / Phase 2 |
| Terminated | The Effect of a Diabetes Action Team in Patients Post Infrainguinal Bypass Surgery With and Without Diabetes NCT00456105 | University of British Columbia | N/A |
| Terminated | Safety/Feasibility Study of HBOC-201 in Amputation at/Below Knee From Critical Lower Limb Ischemia NCT00300040 | Biopure Corporation | Phase 2 |
| Completed | Zilver® PTX™ Global Registry NCT01094678 | Cook Group Incorporated | N/A |
| Terminated | Glycemic Control to Prevent Cardiac Morbidity in Vascular Surgery NCT00328094 | Beth Israel Deaconess Medical Center | N/A |
| Completed | RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System NCT00736086 | Abbott Medical Devices | — |
| Completed | Testosterone for Peripheral Vascular Disease NCT00504712 | Barnsley Hospital | Phase 4 |
| Completed | Testosterone Replacement in Diabetes With Vascular Disease (Version 2) NCT00355537 | Barnsley Hospital | Phase 4 |
| Completed | Study of Hepatocyte Growth Factor (HGF) Via Plasmid Vector to Improve Perfusion in Critical Limb Ischemia Pati NCT00189540 | AnGes USA, Inc. | Phase 2 |
| Completed | Evaluation of Fibrin Sealant 2 in Vascular Surgical Procedures NCT00154141 | Ethicon, Inc. | Phase 3 |
| Completed | Trial of VLTS-934 in Subjects With Intermittent Claudication Secondary to Peripheral Arterial Disease NCT00113009 | Valentis | Phase 2 |
| Completed | Safety and Efficacy Study of Ad2/Hypoxia Inducible Factor (HIF)-1α/VP16 Gene Transfer in Patients With Intermi NCT00117650 | Genzyme, a Sanofi Company | Phase 2 |
| Terminated | Prime Time for Superficial Femoral Artery (SFA) - The SFA Study NCT00902317 | Arizona Heart Institute | N/A |
| Completed | Stem Cell Injection for Peripheral Vascular Disease NCT00278603 | Northwestern University | Phase 1 |
| Completed | Systematic Assessment of Vascular Risk NCT00378040 | University Health Network, Toronto | — |
| Completed | The Dose Response of Niacin ER/Lovastatin on Peak Walking Time (PWT) in Patients With Intermittent Claudicatio NCT00071266 | Kos Pharmaceuticals | Phase 3 |
| Completed | Evaluation of the Efficacy of Rosuvastatin in Daily Practice in Untreated High Risk Patients (CHALLENGE) NCT00574782 | AstraZeneca | — |
| Completed | Trial of VLTS-589 in Subjects With Intermittent Claudication NCT00068133 | Valentis | Phase 2 |
| Terminated | Balloon Angioplasty vs. Cutting Balloon Angioplasty of Femoropopliteal Arteries- a Randomized Controlled Trial NCT00437905 | Medical University of Vienna | Phase 4 |
| Completed | Assessment of the Efficacy of Rosuvastatin in Patient Groups With a Dissimilar Risk Profile in an Observationa NCT00660764 | AstraZeneca | — |
| Completed | Study of HGF Via Plasmid Vector to Improve Perfusion in Critical Limb Ischemia NCT00060892 | AnGes USA, Inc. | Phase 2 |
| Completed | Efficacy and Safety of NM-702 Tablets for the Treatment of Intermittent Claudication NCT00102050 | Nissan Chemical Industries | Phase 2 |
| Terminated | Effects of Remodulin in Patients With Critical Limb Ischemia Following a Vein Bypass Graft NCT00067041 | United Therapeutics | Phase 2 / Phase 3 |
| Completed | Magnevist® Injection Enhanced MRA at Two Dose Levels Compared to Non Contrast MRA for the Detection of Structu NCT00185276 | Bayer | Phase 3 |
| Unknown | Prostaglandin E1 (Liprostin) Treatment With Lower Limb Angioplasty for Peripheral Arterial Occlusive Disease NCT00053716 | Endovasc | Phase 2 |
| Terminated | Study of Remodulin in Patients With Critical Limb Ischemia With No Planned Revascularization Procedures NCT00060996 | United Therapeutics | Phase 3 |
| Completed | Association of Long-term Conditions With Survival Following Heart Attack in England and Wales NCT03037255 | Marlous Hall | — |
| Completed | Effect of Niacin ER/Lovastatin on Peak Walking Time & Claudication Onset Time in Patients With Intermittent Cl NCT00062556 | Kos Pharmaceuticals | Phase 3 |
| Completed | Establish The Benefits Of Using Various Starting Doses Of Atorvastatin On Achievement Of Cholesterol Targets ( NCT00442845 | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. | Phase 4 |
| Completed | Benefits Of Using Various Starting Doses Of Atorvastatin On Achievement Of Cholesterol Targets NCT00442325 | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. | Phase 4 |
| Completed | Efficacy/Safety of Ecraprost in Lipid Emulsion for Treatment of Critical Leg Ischemia Due to Peripheral Arteri NCT00059657 | Tanabe Pharma Corporation | Phase 3 |
| Terminated | Efficacy/Safety of Ecraprost in Lipid Emulsion for Treatment of Critical Leg Ischemia Due to Peripheral Arteri NCT00059644 | Tanabe Pharma Corporation | Phase 3 |
| Completed | Oslo Balloon Angioplasty Versus Conservative Treatment NCT00222196 | Ullevaal University Hospital | N/A |
| Completed | Extract of Ginkgo Biloba (EGB 761) and Vascular Function NCT00029991 | National Center for Complementary and Integrative Health (NCCIH) | Phase 1 / Phase 2 |
| Completed | Magnetic Resonance Imaging to Detect Blood Vessel Inflammation in Patients Undergoing Peripheral Balloon Angio NCT00004549 | National Heart, Lung, and Blood Institute (NHLBI) | Phase 1 |
| Enrolling By Invitation | Registry of Cardiovascular Disease Patients NCT01759225 | Maccabi Healthcare Services, Israel | — |
| Unknown | New Anastomotic Device for End to End Vascular Anastomosis in the Treatment of Peripheral Vascular Disease NCT01514916 | Ab Medica Spa | N/A |