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Clinical Trial Summary

The Cardiac Lead Assessment Study (CLAS) is designed as a prospective, non-randomized, multi-center, international postmarket surveillance study under 522 Order PS120111 (August 16, 2012).


Clinical Trial Description

The objective of this study was to determine the prevalence and incidence of externalized conductors and other visual lead anomalies (as evidenced by imaging) and the risk of progression to electrical dysfunction in subjects with one or more of the following St. Jude Medical (SJM) cardiac leads: Riata leads, Riata ST leads, Durata and/or QuickSite/QuickFlex Cardiac Resynchronization Therapy (CRT) leads. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01507987
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date March 2013
Completion date September 2019