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Trials / Completed

CompletedNCT01088672

Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Stryker Neurovascular · Industry
Sex
All
Age
18 Years – 79 Years
Healthy volunteers
Not accepted

Summary

To determine the revascularization rate of the CE-marked Trevo device in large vessel occlusions in ischemic stroke patients. * Revascularization, defined as at least TICI 2a in the vascular territory treated at end of the neuro interventional procedure.

Detailed description

* Clinical outcomes at 90 days * Mortality at 90 days * Device-related serious adverse events (DRSAEs) * Symptomatic ICH rate within 24 (-6/+12) hours post-procedure

Conditions

Interventions

TypeNameDescription
PROCEDUREMechanical ThrombectomyThe Trevo device is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke.

Timeline

Start date
2010-02-01
Primary completion
2011-08-01
Completion
2011-11-01
First posted
2010-03-17
Last updated
2015-07-17
Results posted
2015-07-17

Locations

7 sites across 4 countries: Austria, Germany, Spain, Sweden

Source: ClinicalTrials.gov record NCT01088672. Inclusion in this directory is not an endorsement.

Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO) (NCT01088672) · Clinical Trials Directory