Automated Detection and Triage of Large Vessel Occlusions Using Artificial Intelligence for Early and Rapid Treatment (ALERT)

Status unconfirmed

Conditions studied: Stroke Workflow and Clinical Outcome Parameters

In brief

Post Market, Prospective, Randomized, Controlled, multi center data collection study to evaluate the use of Viz versus the standard of care in stroke workflow and clinical outcome parameters.

Key facts

Study ID

NCT04142879

Run by

Providence Little Company of Mary-Torrance

People needed

500

Starts

2019-12-01

Expected to finish

2021-12-31

Last updated by the study team

2019-10-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• A subject must meet all of the following inclusion criteria to be included in the study:
• Age of 18 years or greater.
• Signs and symptoms consistent with the diagnosis of a stroke.
• Stroke protocol imaging (CTA) with a confirmed presence of anterior LVO via Viz.

You may not qualify if…

• A subject may not be included in the study if any of the following exclusion criteria are met:
• Poor or incomplete CTA imaging data.
• Disagreement between neuroradiologist and stroke specialist or neurointerventionalist relative to presence of a stroke.
• Other serious, advanced, or terminal illness (investigator judgment) requiring treatment that significantly delays initiating transfer and/or treatment for stroke.

Where it is running

• Providence Little Company of Mary Medical Center-Torrance — Torrance, California, United States

Full record on ClinicalTrials.gov

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