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Search / Trial NCT06289985

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.

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

0 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