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Evaluating Outcomes in the Placement of Boomerang Percutaneous Device

NCT00732628 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2009-02-24

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and effectiveness of the Boomerang percutaneous closure device following diagnostic cerebral angiography or neurointerventional procedures.

Background:

Very few publications have evaluated this relatively novel percutaneous closure device.

Conditions

  • Medical Device
  • Angiography

Interventions

DEVICE

Boomerang closure device

Use of percutaneous of Boomerang closure device. Follow up outcomes evaluated after the use of Boomerang closure device.

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Completion
2008-09-30

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00732628 on ClinicalTrials.gov