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Clinical Trial Summary

This study evaluates the date of the first appropriate and/or inappropriate therapy in patients implanted with a Guidant PRIZM or VITALITY defibrillator and is evaluating eventual predictive risk factors for appropriate/inappropriate therapies as well as the influence of the programmed parameters on these therapies.


Clinical Trial Description

The registry measured the times to, and studied the determinants of, first appropriate (FAT) and inappropriate (FIT) therapy delivered by single, dual and triple chamber (CRT-D) ICD implanted for primary and secondary prevention indications. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00180375
Study type Observational
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date May 2002
Completion date August 2007

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