Study to Assess the Safety and Effectiveness of the Penumbra System
Completed
Phase 2 ResultsSummary of Purpose
This clinical evaluation is a prospective, single-arm, multi-center trial. The purpose of this clinical evaluation is to assess the safety and effectiveness of the Penumbra System in the revascularization of patients presenting with acute ischemic stroke secondary to intracranial, large vessel, occlusive disease.
Read More →Trial Milestones
The following dates are available for this trial. Trial information last updated on 9 January 2009.
| 1 Jun 2006 | 2 Jun 2006 | 1 Jun 2007 | 1 Nov 2007 | 1 Dec 2008 | 20 Nov 2008 |
| Start Date | First Received | 1st Completion | Completion | Verification | Results |
|---|
Trial Design
- Allocation: Non-Randomized
- Masking: Open Label
- Purpose: Treatment
- Endpoint: Safety/Efficacy Study
- Intervention: Single Group Assignment
Contacts
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Jim Pray President Penumbra, Inc. 2401 Merced St., Ste. 200 San Leandro, CA 94577 Telephone: 510-618-3299 Fax: 510-618-3232
jpray@penumbrainc.com
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Recruitment
- Enrollment: 125
- Gender: Both
- Minimum Age: 18 Years
- Accepts Healthy Volunteers: No
- 1 location, 1 country
Principal Investigator
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Marilyn M. Rymer, MD
Marilyn M. Rymer, MD St. Luke's Hospital Kansas City, MO 64111 Phone: 816-932-9847 Email: mrymer@saint-lukes.org
