StrokeNet Thrombectomy Endovascular Platform
Launched by MEDICAL UNIVERSITY OF SOUTH CAROLINA · Mar 1, 2024
Trial Information
Current as of November 02, 2025
Recruiting
Keywords
ClinConnect Summary
The StrokeNet Thrombectomy Endovascular Platform (STEP) trial is studying how to improve treatment for patients experiencing an acute ischemic stroke (AIS), which happens when a blood vessel in the brain is blocked. This trial is specifically looking at patients who have either large or medium vessel occlusions, which means their strokes are caused by blockages in significant blood vessels in the brain. The trial is currently recruiting participants aged 65 and older, but younger adults can also be included if they meet specific criteria.
To be eligible for the trial, participants must have a suspected acute ischemic stroke and show likely signs of a significant blockage in their brain's blood vessels. They should also arrive at the hospital within 24 hours of their last known well time. However, some people may not be able to join the study, such as those with certain medical conditions or those who have had serious allergic reactions to contrast materials used in imaging. Participants in the trial can expect to receive advanced care and treatment options aimed at restoring blood flow to the brain, which is crucial for recovery. This trial aims to better understand and optimize these treatment methods, contributing to improved outcomes for stroke patients.
Gender
ALL
Eligibility criteria
- STEP PLATFORM INCLUSION CRITERIA:
- • 1. Suspected diagnosis acute ischemic stroke
- • 2. Likely causative intracranial large or medium vessel occlusion
- STEP PLATFORM EXCLUSION CRITERIA:
- • 1. Proven contraindication to endovascular thrombectomy
- • 2. Prisoners/incarcerated
- DOMAIN-SPECIFIC ELIGIBILITY CRITERIA:
- • Each domain may have additional eligibility criteria.
- STEP EVT INDICATION EXPANSION DOMAIN INCLUSION CRITERIA:
- 1. Age 18 years or older 2. Pre-stroke modified Rankin Scale score 0-2 3. Presentation to enrolling hospital within 24 hours of last known well/stroke onset 4. Has one of the following presentations:
- 1. LVO patients with mild deficits/low NIHSS (must have both):
- • 1. Mild presenting neurologic deficits - NIHSS 0-5
- • 2. Occlusion of the intracranial Internal Carotid Artery (ICA) or M1 Middle Cerebral Artery (MCA)
- 2. Medium/Distal Vessel Occlusion (must have all 4):
- • 1. Visualized occlusion or perfusion deficit supportive of a cortical branch occlusion (10 cc volume of Tmax \>4s) in one of the following vessels: i) Non-dominant/Co-dominant M2 (defined as serving \< 50% of entire overall MCA territory) ii) M3 iii) M4 iv) A1 v) A2 vi) A3 vii) P1 viii) P2 ix) P3
- • 2. Less than 50% core in the territory supplied by the occluded vessel as evident by hypodensity and loss of grey-white border on NCCT or ADC \<620 mm2/s on diffusion MRI or rCBF\<30% on CTP after 6h of symptom onset.
- • 3. NIHSS \> 4 or NIHSS 2-3 with clearly disabling deficits at presentation to enrolling hospital
- • 4. Able to initiate arterial puncture within 2 hours from qualifying CTA/MRA or CTP/MRP imaging.
- • CT/MR and qualifying CTA/MRA or CTP/MRP should be repeated if more than 120 minutes have elapsed since the imaging and randomization has not been performed.
- STEP EVT INDICATION EXPANSION DOMAIN EXCLUSION CRITERIA:
- • 1. Clinical
- • 1. Presumed septic embolus; suspicion of bacterial endocarditis
- • 2. Seizure at stroke onset or between onset and enrollment
- • 3. Known anaphylactic reaction to contrast material that precludes endovascular reperfusion therapy
- • 4. Intracranial occlusion suspected to be chronic, based on history and/or imaging
- • 5. Intracranial dissection, based on history and/or imaging
- • 6. Cerebral vasculitis, based on history and/or imaging
- • 7. Known pregnancy
- • 8. Known pre-existing medical, neurological or psychiatric disease that would confound the neurological or functional evaluations
- • 9. Known serious, advanced, or terminal illness or life expectancy less than 6 months in the investigator judgment
- • 2. Laboratory
- • a. Known platelet count \<100,000/uL
- • 3. Imaging
- • 1. CT ASPECT score \<6 (MRI ASPECT score \<7)
- • 2. Unfavorable vascular anatomy that limits access to the occluded artery precluding endovascular reperfusion therapy.
- • 3. Acute occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
- • 4. Significant mass effect with midline shift (\>5mm)
- • 5. Evidence of intra-axial tumor (except small meningioma)
- • 6. Evidence of acute intracranial hemorrhage
About Medical University Of South Carolina
The Medical University of South Carolina (MUSC) is a leading academic health center dedicated to advancing medical research and improving patient care through innovative clinical trials. With a strong emphasis on translational medicine, MUSC leverages its extensive resources and expertise to facilitate groundbreaking studies across various medical disciplines. The institution is committed to fostering collaboration among researchers, healthcare professionals, and patients, ensuring that cutting-edge discoveries translate into effective treatments. As a pioneer in health education and research, MUSC plays a vital role in shaping the future of medicine and enhancing health outcomes in the community and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Philadelphia, Pennsylvania, United States
Boston, Massachusetts, United States
Bronx, New York, United States
Providence, Rhode Island, United States
Boston, Massachusetts, United States
Camden, New Jersey, United States
Seattle, Washington, United States
Miami, Florida, United States
Cleveland, Ohio, United States
Chicago, Illinois, United States
San Antonio, Texas, United States
Tampa, Florida, United States
Winston Salem, North Carolina, United States
Birmingham, Alabama, United States
Los Angeles, California, United States
St. Louis, Missouri, United States
Cincinnati, Ohio, United States
Hartford, Connecticut, United States
Stony Brook, New York, United States
Atlanta, Georgia, United States
Pittsburgh, Pennsylvania, United States
Los Angeles, California, United States
Buffalo, New York, United States
Houston, Texas, United States
Iowa City, Iowa, United States
Saint Louis, Missouri, United States
Stanford, California, United States
Charlotte, North Carolina, United States
New York, New York, United States
Charleston, South Carolina, United States
San Diego, California, United States
Columbus, Ohio, United States
Salt Lake City, Utah, United States
New Haven, Connecticut, United States
Cleveland, Ohio, United States
Plano, Texas, United States
Edina, Minnesota, United States
Minneapolis, Minnesota, United States
La Jolla, California, United States
Charlottesville, Virginia, United States
Brooklyn, New York, United States
Pittsburgh, Pennsylvania, United States
Patients applied
Trial Officials
Jordan J Elm, PhD
Principal Investigator
Medical University of South Carolina
Eva A Mistry, MBBS, MSCI
Principal Investigator
University of Cincinnati
Pooja Khatri, MD
Principal Investigator
University of Cincinnati
Colin P Derdeyn, MD
Principal Investigator
University of Virginia
Jeffery L Saver, MD
Principal Investigator
University of California, Los Angeles
Tudor G Jovin, MD
Principal Investigator
The Cooper Health System
Raul G Nogueira, MD, FAHA
Principal Investigator
University of Pittsburgh
David Fiorella, MD, PhD
Principal Investigator
Stony Brook University
Adnan Siddiqui, MD, PhD
Principal Investigator
University at Buffalo
J Mocco, MD, MS
Principal Investigator
MOUNT SINAI HOSPITAL
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported