Angio-Seal Evolution Device Registry

Status Completed

Clinical Trial Summary

Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.

Clinical Trial Description

This multi-center clinical registry is designed to collect data on the use of the Angio-Seal Evolution Device in patients who have had diagnostic and/or interventional procedures through femoral artery access. Data will be collected on a patient's initial screening through hospital discharge and 30 days post-procedure to evaluate major and minor vascular complications as defined in the protocol. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00817349
Study type	Observational
Source	Abbott Medical Devices
Contact
Status	Completed
Phase
Start date	July 2008
Completion date	April 2010

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