CompletedNot Applicable

Angio-Seal Evolution Device Registry

United States1,004 participantsStarted 2008-07

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

Collect major vascular complications

Timeframe: 30 days post-procedure

Trial details

NCT IDNCT00817349

SponsorAbbott Medical Devices

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2010-04

View on ClinicalTrials.gov More Peripheral Vascular Disease trials