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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Mechanical Thrombectomy | Thrombectomy 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.