Medtronic Endovascular clinical trials

A division of Medtronic

The registry lists 51 studies whose lead sponsor is Medtronic Endovascular. 3 are recruiting or about to start. Per ClinicalTrials.gov, last updated Oct 15, 2026.

Studies

Recruiting first, then most recently updated. Showing 50 of 51. List all 51 → · All Medtronic studies →

• Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Detachable CoilsEnrolling by invitationNCT07639853

  Sponsor listed in the registry: Medtronic Endovascular

• Onyx™ Liquid Embolic IDE Clinical StudyRecruitingNCT06742801Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectomy SystemRecruitingNCT07335341

  Sponsor listed in the registry: Medtronic Endovascular

• VenaSeal Spectrum: Global Post-Market Randomized Controlled TrialTerminatedNCT03820947Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Ellipsys Vascular Access System Post Market Surveillance (PS) StudyCompletedNCT04484220Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. PTACompletedNCT02963649Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease and Critical Limb IschemiaTerminatedNCT04120610

  Sponsor listed in the registry: Medtronic Endovascular

• IN.PACT™ AV Access IDE StudyCompletedNCT03041467Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• ABRE Clinical Study of the Abre Venous Self-expanding Stent SystemCompletedNCT03038438Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy SystemTerminatedNCT04494035Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• CAPERE Thrombectomy System Post-Market Clinical Follow Up StudyTerminatedNCT03869645

  Sponsor listed in the registry: Medtronic Endovascular

• Percutaneous Less Invasive AV Fistula for Vascular Access in ESRDCompletedNCT02363972Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) TrialCompletedNCT00619775Phase 3

  Sponsor listed in the registry: Medtronic Endovascular

• Study to Evaluate the Effect of Simvastatin, Losartan and Pioglitazone on Patients With Peripheral Arterial Disease.CompletedNCT00720577Early Phase 1

  Sponsor listed in the registry: Medtronic Endovascular

• Pivotal Study of the Medtronic Axys EX Rotational Atherectomy SystemWithdrawnNCT04282161Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• IN.PACT Global Clinical StudyCompletedNCT01609296Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Ellipsys Vascular Access System RegistryCompletedNCT03454113

  Sponsor listed in the registry: Medtronic Endovascular

• Catheter System Feasibility Clinical TrialCompletedNCT02816398Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• EverFlex Post Approval StudyCompletedNCT01680835Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Study of SilverHawk®/TurboHawk® in Lower Extremity Vessels (DEFINITIVE™ LE)CompletedNCT00883246Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial DiseaseCompletedNCT01366482Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• TurboHawk™ Japan Trial in Patients With PADCompletedNCT02169921Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• VeClose Five Year Follow-Up Extension StudyCompletedNCT03455699

  Sponsor listed in the registry: Medtronic Endovascular

• Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval StudyCompletedNCT00530504Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinical StudyCompletedNCT02066740Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Rapid Renal Sympathetic Denervation for Resistant HypertensionCompletedNCT01520506Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-popliteal AtherosclerosisCompletedNCT00530712Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• IN.PACT Admiral Drug-Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Superficial Femoral Artery (SFA) and Proximal Popliteal Artery (PPA)CompletedNCT01566461Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• MDT-2113 Drug-Eluting Balloon vs. Standard PTA for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery and/or Proximal Popliteal ArteryCompletedNCT01947478Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• VenaSeal Sapheon Closure System Pivotal Study (VeClose)CompletedNCT01807585Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• ClosureFAST - Radiofrequency Great Saphenous Vein TreatmentCompletedNCT00842296Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• DURABILITY™ Iliac StudyCompletedNCT01400919Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• VISIBILITY™ Iliac StudyCompletedNCT01402700Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treatment of Below the Knee Critical Limb IschemiaCompletedNCT00941733Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter, Single-Blinded, Randomized Study.CompletedNCT00509392Phase 4

  Sponsor listed in the registry: Medtronic Endovascular

• Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for the Treatment of SFA and Proximal Popliteal Arterial DiseaseCompletedNCT01175850Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• RFS (Radiofrequency Stylet) - Radiofrequency Perforator Vein Treatment StudyTerminatedNCT01079598Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery and/or Proximal Popliteal Artery Using the IN.PACT Admiral™ Drug-Eluting Balloon in a Chinese Patient PopulationCompletedNCT02118532Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• European Sapheon™ Closure System Observational ProspectivE (eSCOPE) StudyCompletedNCT01570101Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• The Sapheon Closure System Feasibility StudyCompletedNCT01603433Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• The Complete® SE SFA Study for the Treatment of SFA/PPA LesionsCompletedNCT00814970Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• The Complete® Self-Expanding Stent and Stent Delivery System RegistryCompletedNCT00730730Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) StudyCompletedNCT00753337Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE)CompletedNCT00880230Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• Proximal Protection With The Mo.Ma Device During Carotid StentingCompletedNCT00744523Not applicable

  Sponsor listed in the registry: Medtronic Endovascular

• DEFINITIVE AR Two Year Follow-up Extension StudyCompletedNCT02363894

  Sponsor listed in the registry: Medtronic Endovascular

• Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections StudyTerminatedNCT01341483

  Sponsor listed in the registry: Medtronic Endovascular

• OneShot Renal Denervation RegistryTerminatedNCT01844037Phase 2/3

  Sponsor listed in the registry: Medtronic Endovascular

• Study of the SilverHawk™ /TurboHawk™ Plaque Excision Systems Used With SpiderFX to Treat Calcified Peripheral Arterial Disease (DEFINITIVE Ca++)CompletedNCT00733135Phase 2/3

  Sponsor listed in the registry: Medtronic Endovascular

• Rapid Renal Sympathetic Denervation for Resistant Hypertension IIWithdrawnNCT01939392Phase 2/3

  Sponsor listed in the registry: Medtronic Endovascular