Trials / Completed
CompletedNCT00817349
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,004 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.
Detailed 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.
Conditions
- Peripheral Vascular Disease
- Coronary Artery Disease
- Peripheral Artery Disease
- Arterial Occlusive Disease
- Coronary Heart Disease
Timeline
- Start date
- 2008-07-01
- Primary completion
- 2010-04-01
- Completion
- 2010-04-01
- First posted
- 2009-01-06
- Last updated
- 2019-02-04
Locations
10 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00817349. Inclusion in this directory is not an endorsement.