Clinical Trials Directory

Trials / Completed

CompletedNCT00478478

Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic Stroke

Status
Completed
Phase
Study type
Observational
Enrollment
1,000 (actual)
Sponsor
Stryker Neurovascular · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Post-Market Registry on Use of Merci Retrieval System. Primary data to be collected will include: * Post-procedure revascularization success * 90-day mRS 0-2 * 90-day mortality

Detailed description

The Merci Registry is a prospective multicenter registry with up to 3000 patients enrolled at a maximum of 100 sites. The registry requires use (at least one pass in the intracranial vasculature) of any Merci Retriever device (X Series, L Series, V Series) in the setting of acute ischemic stroke due to large vessel intracranial occlusion.

Conditions

Interventions

TypeNameDescription
PROCEDUREMechanical ThrombectomyThrombectomy performed with the Merci Retriever in the setting of acute ischemic stroke.

Timeline

Start date
2007-06-01
Primary completion
2010-05-01
Completion
2010-09-01
First posted
2007-05-24
Last updated
2014-11-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00478478. Inclusion in this directory is not an endorsement.