Safety and Efficacy Study of RENEWAL 4 AVT
NCT00180336 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 170
Last updated 2007-06-25
Summary
The purpose of this study is to assess the safety and effectiveness of the CONTAK RENEWAL 4 AVT device.
Conditions
- Heart Failure
- Tachycardia
- Atrial Fibrillation
- Atrial Flutter
- Ventricular Fibrillation
Interventions
- DEVICE
-
CRT-D
Sponsors & Collaborators
-
Boston Scientific Corporation
lead INDUSTRY
Principal Investigators
-
Johannes Sperzel, MD · Kerckhoff Klinik Bad Nauheim (Germany)
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-07-31
Countries
- Germany
Study Locations
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