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

Stryker Neurovascular1,000 enrolled

Overview

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

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.

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Ischemic Stroke

Interventions

Mechanical ThrombectomyPROCEDURE

Thrombectomy performed with the Merci Retriever in the setting of acute ischemic stroke.

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Patient with ischemic stroke is treated with a Merci Retriever that is indicated for thrombus removal in ischemic stroke. "Treated" is defined as being when a Merci Retriever is deployed in the neurovasculature of a patient with an ischemic stroke * Patient/patient's surrogate provides informed consent and is willing to comply with the protocol requirements and complete required clinical evaluations, or in the absence of informed consent, an IRB/EC approved waiver of consent and executed data use agreement are in place Exclusion Criteria: -There are no exclusion criteria for this protocol

Locations (1)

St. Luke's Brain and Stroke Institute

Kansas City, Missouri, United States

Outcomes

Primary Outcomes

Post-procedure revascularization success

Time frame: post-procedure

Secondary Outcomes

NIHSS change from baseline to 24-hours

Time frame: 24-hour

90-day mRS outcomes

Time frame: 90-day

90-day mortality

Time frame: 90-day

Data from ClinicalTrials.gov

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