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Sponsored by: |
Concentric Medical |
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Information provided by: | Concentric Medical |
ClinicalTrials.gov Identifier: | NCT00318071 |
The primary objectives of the Multi MERCI trial were:
Condition | Intervention |
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Ischemic Stroke |
Device: Merci Retriever |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study |
Official Title: | A Multinational Controlled Registry to Evaluate the Concentric Merci Retriever System (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) |
Enrollment: | 164 |
Study Start Date: | January 2004 |
Study Completion Date: | December 2006 |
Primary Completion Date: | December 2006 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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Treatment: Experimental
Treatment arm patients had at least one Merci Retriever deployed
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Device: Merci Retriever |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Concentric Medical |
Study ID Numbers: | INT-LR-001 |
Study First Received: | July 14, 2005 |
Last Updated: | April 15, 2008 |
ClinicalTrials.gov Identifier: | NCT00318071 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Stroke Ischemic Thrombus Embolectomy Thrombectomy |
Merci Concentric Embolus Embolism Mechanical |
Cerebral Infarction Embolism Stroke Vascular Diseases Central Nervous System Diseases Brain Ischemia |
Brain Infarction Ischemia Brain Diseases Infarction Cerebrovascular Disorders Thrombosis |
Cerebral Infarction Stroke Nervous System Diseases Vascular Diseases Central Nervous System Diseases |
Brain Ischemia Cardiovascular Diseases Brain Infarction Brain Diseases Cerebrovascular Disorders |