Groin Complications Post Percutaneous Coronary Intervention Using Either Manual Compression or PERCLOSE Device

NCT00842179 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2517

Last updated 2009-02-12

No results posted yet for this study

Summary

The objective of this study is to compare groin complication rates in low and high risk patients post percutaneous coronary intervention (PCI) closed by either a 6 French Perclose vascular closure device (VCD) or manual compression.

Conditions

  • Vascular Closure

Sponsors & Collaborators

  • Abbott Medical Devices

    collaborator INDUSTRY
  • Clinyx, LLC

    lead OTHER

Principal Investigators

  • Jonathan Roberts, MD · Baptist Health South Florida

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2008-10-31
Completion
2008-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00842179 on ClinicalTrials.gov