SOURCE XT REGISTRY

Status Completed

Clinical Trial Summary

This registry is to expand upon existing data sets, to identify patient characteristics and indicators related to complications and clinical benefits for patients with symptomatic severe calcific degenerative aortic stenosis that are undergoing treatment with the commercially available Edwards SAPIEN XT™ Valve, and delivery devices.

Clinical Trial Description

Consecutive patient data should be collected at discharge, 30 days and 12 months post-implant. Subsets of patients may undergo additional follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01238497
Study type	Observational
Source	Edwards Lifesciences
Contact
Status	Completed
Phase
Start date	September 2010
Completion date	November 2016

View Details

See also
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