Medtronic: Peripheral Arterial Disease trials

The registry lists 24 Peripheral Arterial Disease studies with Medtronic as lead sponsor. 2 are open to participants now and 15 have results posted.

Early Phase 1 1Phase 2 2Phase 3 1Phase 4 1No phase 20(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Detachable CoilsEnrolling by invitationNCT07639853
• Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectomy SystemRecruitingNCT07335341
• FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease and Critical Limb IschemiaTerminatedNCT04120610Results posted
• IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. PTACompletedNCT02963649Not applicableResults posted
• EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinical StudyCompletedNCT02066740Not applicableResults posted
• EverFlex Post Approval StudyCompletedNCT01680835Not applicableResults posted
• IN.PACT Global Clinical StudyCompletedNCT01609296Not applicableResults posted
• VISIBILITY™ Iliac StudyCompletedNCT01402700Not applicableResults posted
• DURABILITY™ Iliac StudyCompletedNCT01400919Not applicableResults posted
• Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for the Treatment of SFA and Proximal Popliteal Arterial DiseaseCompletedNCT01175850Not applicableResults posted
• Study of SilverHawk®/TurboHawk® in Lower Extremity Vessels (DEFINITIVE™ LE)CompletedNCT00883246Not applicableResults posted
• Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE)CompletedNCT00880230Not applicableResults posted
• The Complete® SE SFA Study for the Treatment of SFA/PPA LesionsCompletedNCT00814970Not applicableResults posted
• The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) StudyCompletedNCT00753337Not applicableResults posted
• Study of the SilverHawk™ /TurboHawk™ Plaque Excision Systems Used With SpiderFX to Treat Calcified Peripheral Arterial Disease (DEFINITIVE Ca++)CompletedNCT00733135Phase 2/3Results posted
• The Complete® Self-Expanding Stent and Stent Delivery System RegistryCompletedNCT00730730Not applicableResults posted
• Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-popliteal AtherosclerosisCompletedNCT00530712Not applicableResults posted
• Pivotal Study of the Medtronic Axys EX Rotational Atherectomy SystemWithdrawnNCT04282161Not applicable
• DEFINITIVE AR Two Year Follow-up Extension StudyCompletedNCT02363894
• TurboHawk™ Japan Trial in Patients With PADCompletedNCT02169921Not applicable
• Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial DiseaseCompletedNCT01366482Not applicable
• Study to Evaluate the Effect of Simvastatin, Losartan and Pioglitazone on Patients With Peripheral Arterial Disease.CompletedNCT00720577Early Phase 1
• A Non-Randomized Study of the NightHawk Peripheral Plaque Excision System During Plaque Excision of Peripheral Arterial DiseaseTerminatedNCT00516308Phase 2
• Plaque Removal Versus Open Bypass Surgery For Critical Limb IschemiaTerminatedNCT00504088Phase 4