Angio-Seal Evolution Device Registry

Abbott

Status: Completed

Conditions: Coronary Artery Disease; Coronary Heart Disease; Peripheral Artery Disease; Peripheral Vascular Disease; Arterial Occlusive Disease

Study type: Observational

Funder types: Industry

Identifiers

NCT00817349

0801

Details and patient eligibility

About

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

Full 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.

Enrollment: 1,004 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient is having a diagnostic and/or interventional procedure via femoral artery access.

Exclusion criteria

• Patients who are unable to provide written informed consent.