BARD® Study of LIFESTREAM™ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease
NCT02228564
Arterial Occlusive Disease, Arterial Occlusive Diseases
Little Rock, Arkansas, United States
View Trial DetailsNCT Number: NCT00817349
Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.
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Notify Me18 year and older
All sexes
Observational
Good Samaritan Hospital, Los Angeles, California, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 30 days post-procedure
Time frame: Immediately following procedure
Time frame: 30 days post-procedure
Abbott Medical Devices
Industry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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