Evaluating Outcomes in the Placement of Boomerang Percutaneous Device

Stopped early

Conditions studied: Medical Device, Angiography

In brief

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.

Key facts

Study ID

NCT00732628

Run by

University of Michigan

People needed

200

Starts

2008-01-01

Expected to finish

2008-09-01

Last updated by the study team

2009-02-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Any patient that has a percutaneous Boomerang closure device placed after having a neuro-intervention

You may not qualify if…

• Patients that do not have this medical device used post procedure

Where it is running

• University of Michigan — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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