Medtronic: Constriction, Pathologic trials

The registry lists 12 Constriction, Pathologic studies with Medtronic as lead sponsor. 0 are open to participants now and 9 have results posted.

Phase 3 1Phase 4 3No phase 8(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.

• Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Symptomatic Severe Aortic StenosisCompletedNCT01634269Not applicableResults posted
• IN.PACT Admiral Drug-Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Superficial Femoral Artery (SFA) and Proximal Popliteal Artery (PPA)CompletedNCT01566461Not applicableResults posted
• Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve ReplacementCompletedNCT01531374Not applicableResults posted
• Clinical Evaluation of MDT-2111 in Subjects With Symptomatic Severe Aortic StenosisCompletedNCT01437098Not applicableResults posted
• Neurogenic Intermittent Claudication Evaluation StudyCompletedNCT00905359Phase 4Results posted
• Intermittent Neurogenic Claudication Treatment With APERIUS®CompletedNCT00887744Phase 4Results posted
• DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolateral FusionTerminatedNCT00627497Phase 3Results posted
• Long-Term Outcomes for Lumbar Spinal Stenosis Patients Treated With X STOP®CompletedNCT00534092Results posted
• Condition of Approval StudyTerminatedNCT00517751Phase 4Results posted
• Evolut™ EXPAND TAVR II Pivotal TrialActive, not recruitingNCT05149755Not applicable
• 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
• Post-Approval Study for the MOSAIC® BioprosthesesCompletedNCT01574625