Boston Scientific Corporation: Ventricular Fibrillation trials
The registry lists 18 Ventricular Fibrillation studies with Boston Scientific Corporation as lead sponsor. 0 are open to participants now and 6 have results posted.
Phase 2 2Phase 3 2Phase 4 1No phase 15(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.
- Acute Feasibility Investigation of a New S-ICD ElectrodeCompletedNCT03802110Not applicableResults posted
- Understanding Outcomes With the EMBLEM™ S-ICD in Primary Prevention Patients With Low Ejection FractionCompletedNCT02433379Not applicableResults posted
- Safety and Performance Study of the RELIANCE 4-Front Passive Fixation LeadCompletedNCT01856491Not applicableResults posted
- Shockless Implant EvaluationCompletedNCT00800384Not applicableResults posted
- SAFEty of Two Strategies of ICD Management at ImplantationCompletedNCT00661037Results posted
- Septal - Success Rate and Clinical Outcome of Septal Implant of Ventricular Defibrillation LeadCompletedNCT00180297Not applicableResults posted
- First Arrhythmia Collection of Transvenous and Simultaneous Subcutaneous Implantable Defibrillator DataCompletedNCT01161589
- Canadian Registry of ICD Implant Testing ProceduresCompletedNCT00848341
- Comparison of Right Ventricular Septal and Right Ventricular Apical Pacing in Patients Receiving a CRT-D DeviceCompletedNCT00833352Not applicable
- Feature Assessment Study for Indications Based ProgrammingCompletedNCT00711893
- Cognis and Teligen 100 HE and Reliance Quadripolar Defibrillation Lead (4-Site) Field FollowingCompletedNCT00606710
- Further Acute Research of a Subcutaneous Implantable Defibrillator (S-ICD) SystemCompletedNCT00399217
- Safety and Effectiveness of Cardiac Resynchronization Therapy With DefibrillationCompletedNCT00387803Phase 2/3
- INSURE: INcidence Free SUrvival Before and After Implantable Cardioverter Defibrillator (ICD) ReplacementCompletedNCT00180440
- VERRARI - "Are Ventricular Arrhythmic Episodes Reduced by Rate Response in ICDs?"CompletedNCT00180427Phase 4
- OPERA: French Observational Study on Patients Implanted With a Guidant PRIZM or Vitality DefibrillatorCompletedNCT00180375
- Leader - Evaluation of Endotak RelianceCompletedNCT00180349
- Safety and Efficacy Study of RENEWAL 4 AVTCompletedNCT00180336Phase 2/3