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Sentinel(TM) Post-Market Registry

Transcatheter Aortic Valve Replacement Clinical Trial

Official title:
Histopathology of Embolic Debris Captured During Transcatheter Aortic Valve Replacement

Clinical Trial Summary

The SENTINEL Post-Market Registry is a prospective, multi-center, registry using the CE-Marked Sentinel System in subjects with severe symptomatic calcified native aortic valve stenosis indicated for TAVR.

Subjects enrolled in the registry will undergo TAVR + Sentinel. Basic demographic information and detailed procedural data will be captured and documented in a registry case report form.

All Sentinel filters will be sent for histopathology at an independent core-lab.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Aortic Valve Stenosis
  • Severe Symptomatic Calcified Native Aortic Valve Stenosis
  • Transcatheter Aortic Valve Replacement
Clinical Trial Details
NCT number NCT02255851
Study type Observational [Patient Registry]
Source Claret Medical
Contact
Status Completed
Phase
Start date March 2014
Completion date May 2016
View Details
See also
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