Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemic Stroke (STRATIS) Registry
Completed
Conditions studied: Ischemic Stroke
In brief
The purpose of this registry is to assess clinical outcomes, and different factors that may affect these clinical outcomes such as systems of care, associated with the use of Covidien market-released neurothrombectomy devices intended to restore blood flow in patients experiencing acute ischemic stroke due to large intracranial vessel occlusion.
Key facts
- Study ID
- NCT02239640
- Run by
- Medtronic Neurovascular Clinical Affairs
- People needed
- 984
- Starts
- 2014-08-21
- Expected to finish
- 2016-10-07
- Last updated by the study team
- 2019-06-07
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient or patient's legally authorized representative has given Informed Consent according to Good Clinical Practices (GCP) and/or IRB and/or local or institutional policies.
- Patient has experienced an acute ischemic stroke due to large intracranial vessel occlusion (with associated symptoms) and has been or will be treated with a Covidien market-released neurothrombectomy device, as the initial device used to remove the thrombus.
- Treatment within 8 hours of stroke onset.
- Pre-Stroke Modified Rankin Scale (mRS) score ≤ 1 (immediately) prior to stroke onset.
- Pre-treatment National Institutes of Health Stroke Scale (NIHSS) ≥ 8 and ≤ 30.
You may not qualify if…
- Concurrent participation in a multicenter randomized study.
Where it is running
- University of Arizona Medical Center — Tucson, Arizona, United States
- University of California Irvine — Irvine, California, United States
- University of California Los Angeles — Los Angeles, California, United States
- Mercy San Juan Medical Center/ Mercy General — Sacramento, California, United States
- California Pacific Medical Center — San Francisco, California, United States
- Los Robles Medical Center — Thousand Oaks, California, United States
- Advanced Neuroscience Network/Tenet South Florida — Delray Beach, Florida, United States
- South Broward Hospital — Hollywood, Florida, United States
- Baptist Medical Center - Jacksonville — Jacksonville, Florida, United States
- University of Miami Hospital — Miami, Florida, United States
- Baptist Hospital of Miami — Miami, Florida, United States
- Florida Hospital — Orlando, Florida, United States
- Grady Memorial Hospital — Atlanta, Georgia, United States
- WellStar Kennestone Regional Medical Center — Marietta, Georgia, United States
- Presence St. Joseph Medical Center — Joliet, Illinois, United States
- Advocate Christ Medical Center — Oak Lawn, Illinois, United States
- Baptist Health Lexington/Central Baptist — Lexington, Kentucky, United States
- University of Kentucky Hospital — Lexington, Kentucky, United States
- Baptist Hospital Louisville — Louisville, Kentucky, United States
- Norton Healthcare — Louisville, Kentucky, United States
- Maine Medical Center — Portland, Maine, United States
- University of Maryland Medical Center — Baltimore, Maryland, United States
- Brigham and Women's Hospital — Boston, Massachusetts, United States
- University of Massachusetts Memorial Medical Center — Worcester, Massachusetts, United States
- Banner University Medical Center — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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