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Clinical Trial Summary

Primary objective is to evaluate the safety and performance of the implanted Subcutaneous implantable cardioverter defibrillator (S-ICD) system. A maximum of 10 subjects were to be enrolled and followed for one month to collect data on the safety, efficacy, and performance of the implanted S-ICD system. Additionally, patient comfort will be assessed as will cosmetic outcome.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00853645
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date July 2008
Completion date September 2008

See also
  Status Clinical Trial Phase
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Completed NCT01492764 - Ablation of Ventricular Fibrillation by Accurate Targeting of Arrhythmogenic Regions (AVATAR)
Completed NCT01906775 - Sub-threshold Pacing to Prevent Pacemaker-induced Ventricular Tachycardia N/A