Trevo® Retriever Registry Post Market Surveillance

Status Completed

Clinical Trial Summary

The purpose of the Trevo® Retriever Registry is to collect real world performance data of the Trevo Retriever which is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke.

Clinical Trial Description

Trevo Retriever Registry is a prospective, open-label, consecutive enrollment, multi-center, international registry that may enroll a maximum of 2000 patients at up to 100 sites worldwide. Revascularization status will be assessed at the end of the procedure using the modified TICI (Thrombolysis in Cerebral Infarction)score. Additional data collection will include:

1. Day 90 mRS assessment

2. Day 90 all cause mortality

3. Neurological deterioration at 24 hours post procedure, defined as a four or more point increase in the NIHSS score from the baseline score

4. Rates of device and procedure related serious adverse events (AEs) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02040259
Study type	Observational [Patient Registry]
Source	Stryker Neurovascular
Contact
Status	Completed
Phase
Start date	November 25, 2013
Completion date	December 28, 2017

View Details

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