MicroPort Scientific Corporation: all 121 studies
Page 2 of 2. Open to participants first (41), then studies with results posted, then the rest; newest registration first within each.
- Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing InsertsActive, not recruitingNCT02351414
- Triple-site Biventricular Stimulation in the Optimization of CRTCompletedNCT02350842Not applicable
- Clinical and Device Functional Assessment of Real World ICD PatientsCompletedNCT02341768
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® L Revision Femoral StemsActive, not recruitingNCT02314702
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator HA Coated Modular Femoral StemsTerminatedNCT02314611
- Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral StemsTerminatedNCT02309593
- Post Market Clinical Follow-Up Study Protocol for CONSERVE® Press-Fit Femoral ComponentsActive, not recruitingNCT02285842
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral StemsActive, not recruitingNCT02239783
- Safety and Efficacy Study of MicroPort's Transcatheter Aortic Valve and Delivery System for TAVIStatus unknownNCT02221921Not applicable
- Assessment of the MRI Solution: KORA 100 and Beflex Pacing Leads SystemCompletedNCT02175797Not applicable
- Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular ComponentsActive, not recruitingNCT02149667
- Registry of Sleep Apnea Monitoring and Atrial Fibrillation in Pacemaker Patients (RESPIRE)CompletedNCT01922726
- Clinical Assessment of the SonR Algorithm in the PARADYM RF SonR CRT-D by EchocardiographyCompletedNCT01869062Not applicable
- Clinical Trial of the SonRtip Lead and Automatic AV-VV Optimization Algorithm in the PARADYM RF SonR CRT-DStatus unknownNCT01534234Phase 3
- CONSERVE Plus Post-Approval Study (PAS)TerminatedNCT01367899
- EMERALD - AssEssment of CoMorbidities & Atrial ArRhythmiA Burden in DuaL-Chamber PaceD PatientsCompletedNCT01188356
- Efficacy of the ATP Switch Automatic Programming in Implantable Cardioverter Defibrillator (ICD) and Cardiac Resynchronization Therapy Defibrillator (CRT-D) Implanted PatientsTerminatedNCT01169246
- Firebird2 Cobalt-Chromium Alloyed Sirolimus-Eluting Stent Registry TrialStatus unknownNCT00868829Not applicable
- Evaluation of EndoRefix Endovascular Delivery System and StapleWithdrawnNCT00668681Not applicable
- Prospective Aneurysm Trial: High Angle Aorfix™ Bifurcated Stent GraftCompletedNCT00522535Not applicable
- ARBITER-II: Aorfix™ Bifurcated Safety and Performance Trial: Phase II, Angulated VesselsCompletedNCT00442065Phase 2/3