Status:
TERMINATED
Evaluating Outcomes in the Placement of Boomerang Percutaneous Device
Lead Sponsor:
University of Michigan
Conditions:
Medical Device
Angiography
Eligibility:
All Genders
18+ years
Brief 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. Backgro...
Detailed Description
The purpose of this study is to document our experiences using the Boomerang closure device. Several different closure devices are used in the department of Radiology. A closure device is something th...
Eligibility Criteria
Inclusion
- Any patient that has a percutaneous Boomerang closure device placed after having a neuro-intervention
Exclusion
- Patients that do not have this medical device used post procedure
Key Trial Info
Start Date :
January 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
September 1 2008
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00732628
Start Date
January 1 2008
End Date
September 1 2008
Last Update
February 24 2009
Active Locations (1)
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1
University of Michigan
Ann Arbor, Michigan, United States, 48109