Collecting Information From People Undergoing a Procedure for Treatment of Stroke (ASSIST)
Protocol: SITE00000050
Full Title
ASSIST Registry Protocol
Description
This study enrolls people who have been diagnosed with an ischemic stroke, a type of stroke where an artery in your brain has been blocked by a blood clot. The purpose of this study is to collect information (data) on medical devices used in the procedure to remove the blood clot and look at the success and related to different medical devices.

This study lasts for 90 days and consists of brief follow ups after treatment occurring at 18-48 hours, 5-7 days, 30 days, and 90 days post-procedure. The study involves collecting data from your medical records starting from the time of your first symptoms through your 90-day post-procedure checkup visit. This study takes place at Buffalo General Medical Center/Gates Vascular Institute in Buffalo NY.

Technical Description

This is a prospective, global, consecutive enrollment Registry of anterior circulation acute ischemic stroke patients with a LVO who undergo treatment with one of the interventional techniques using Stryker Neurovascular (SNV) devices for the first pass.
Compensation: No
Eligibility
Adults ages 18+
Diagnosed with ischemic stroke and planning to undergo procedure to remove blood clot
Age Group: Adults
Principal Investigator: ELAD LEVY
ClinicalTrials.gov: Open Study
Contact(s)
JENNIFER GAY
jgay@ubns.com
+1 716-888-4811
Want to Learn More?
Let us know how the study team can reach you. If you do not hear back within 2 business days, reach out to the study team directly at the contact information above or email ctsiresearch@buffalo.edu and someone will assist you.