RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System

NCT00736086 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 165

Last updated 2008-08-15

No results posted yet for this study

Summary

To evaluate early ambulation in patients who receive the StarClose™ VCS post-percutaneous diagnostic procedure.

Conditions

Interventions

DEVICE

Vessel Closure (StarClose™)

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • William Kussmaul, MD · Drexel University/Hahnemann

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2006-11-30
Completion
2006-12-31

Countries

  • United States

Study Locations

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Entities

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 NCT00736086 on ClinicalTrials.gov