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Clinical trialNCT01222104CompletedObservational

Angio-Seal Interventional Radiology (IR) Registry

SponsorAbbott Medical DevicesEnrollment634Diagnostic and/or Interventional Radiology Procedures
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to collect data on the standard of care use of the St. Jude Medical (SJM) Angio Seal™ Evolution™ and V-Twist Integrated Platform (VIP) Devices in diagnostic and/or interventional radiology patient populations.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

10 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Loma Linda University Medical Center

    Loma Linda, California, United States

  • Yale New Haven Hospital

    New Haven, Connecticut, United States

  • University of Florida

    Gainesville, Florida, United States

  • Baptist Cardiac and Vascular Institute

    Miami, Florida, United States

  • University of Kansas Medical Center

    Kansas City, Kansas, United States

  • Kaleida Health

    Buffalo, New York, United States

  • Mayfield Clinic, Inc.; the University Hospital

    Cincinnati, Ohio, United States

  • Riverside Methodist Hospital

    Columbus, Ohio, United States

  • Albert Einstein Medical Center

    Philadelphia, Pennsylvania, United States

  • Thomas Jefferson Hospital

    Philadelphia, Pennsylvania, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2010
Primary completion
31 May 2011
Completion
31 May 2011
Last update posted
5 Feb 2019
Registered enrollment
634
Registry id
NCT01222104

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.