Abbott: Peripheral Vascular Diseases trials
The registry lists 16 Peripheral Vascular Diseases studies with Abbott as lead sponsor. 0 are open to participants now and 7 have results posted.
Phase 3 5Phase 4 1No phase 10(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.
- Tissue Removal Assessment With Ultrasound of THe SFA and PoplitealCompletedNCT01938391Not applicableResults posted
- ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbable Vascular Scaffold) SystemCompletedNCT01468974Not applicableResults posted
- Absolute Pro® MOMENTUM™CompletedNCT01444378Not applicableResults posted
- Trial to Evaluate the Safety & Efficacy of the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac ArteryCompletedNCT01396525Phase 3Results posted
- Data Registry Following Patients Using Supera Stent in the Femoral ArteriesTerminatedNCT01154751Not applicableResults posted
- Comparison of the SUpera® PERipheral System in the Superficial Femoral ArteryCompletedNCT00933270Not applicableResults posted
- Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery.CompletedNCT00844532Phase 3Results posted
- Popliteal Artery of Treatment With Balloon Angioplasty vs. SUPERA VERITAS Peripheral Stent SystemWithdrawnNCT01667393Not applicable
- The ABSORB BTK (Below The Knee) Clinical InvestigationTerminatedNCT01341340Not applicable
- Angio-Seal Evolution Device RegistryCompletedNCT00817349
- RISE: A Clinical Evaluation of the StarClose™ Vascular Closure SystemCompletedNCT00736086
- A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral Stent SystemCompletedNCT00475566Not applicable
- ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded ArteriesCompletedNCT00180505Phase 4
- Safety & Efficacy of a Combination Niacin ER/Simvastatin in Patients With Dyslipidemia: A Dose-Ranging Study - SEACOASTCompletedNCT00082251Phase 3
- The Dose Response of Niacin ER/Lovastatin on Peak Walking Time (PWT) in Patients With Intermittent Claudication - TROPICCompletedNCT00071266Phase 3
- Effect of Niacin ER/Lovastatin on Peak Walking Time & Claudication Onset Time in Patients With Intermittent ClaudicationCompletedNCT00062556Phase 3