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NCT Number: NCT06289985

StrokeNet Thrombectomy Endovascular Platform

STEP is a Randomized, Multifactorial, Adaptive Platform trial that seeks to optimize the care of patients with acute ischemic stroke (AIS) due to large (LVO) or medium vessel occlusions (MVO).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama Hospital, Birmingham, Alabama, United States

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About this study

The StrokeNet Thrombectomy Endovascular Platform (STEP) is conducted within NIH StrokeNet at 38 comprehensive stroke centers across the US. The primary goal is to optimize all aspects of care of acute ischemic stroke patients with a large or a medium vessel occlusion. The platform trial operates under an overarching Master Protocol in an inferentially integrated framework. The platform trial is designed to support the studies of three broad categories of therapeutics: expansion of endovascular treatment (EVT) indications, innovative EVT devices and concomitant medical therapies, and novel pre- and early-hospital technologies and systems of care. As new interventions are put forth, they will be added to the Master Protocol as a new Domain or part of an existing Domain. STEP utilizes a flexible Bayesian design with frequent adaptive analyses to assess whether a given intervention is superior, inferior, or equivalent either within a Domain or for specific populations within the Domain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

STEP PLATFORM INCLUSION CRITERIA:

  • Suspected diagnosis acute ischemic stroke
  • Likely causative intracranial large or medium vessel occlusion

STEP PLATFORM EXCLUSION CRITERIA:

  • Proven contraindication to endovascular thrombectomy
  • Prisoners/incarcerated

DOMAIN-SPECIFIC ELIGIBILITY CRITERIA:

Each domain may have additional eligibility criteria.

STEP EVT INDICATION EXPANSION DOMAIN INCLUSION CRITERIA:

  • 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. 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. The exception is for LVO Mild deficit/Low NIHSS 0-5 for which imaging would only need to be repeated if there has been significant improvement in the NIHSS prior to randomization.

  • Has one of the following presentations:
  • LVO patients with mild deficits/low NIHSS (must have both):
  • Mild presenting neurologic deficits - NIHSS 0-5 (Must have some focal neurological deficit attributable to the target occlusion if NIHSS 0)
  • Complete occlusion of the intracranial Internal Carotid Artery (ICA) or M1 Middle Cerebral Artery (MCA)
  • Medium/Distal Vessel Occlusion:
  • Visualized complete occlusion or perfusion deficit (Tmax > 4s) supportive of a cortical branch occlusion in one of the following vessels:

i) Non-dominant/Co-dominant M2 (defined as serving < 50% of entire overall MCA territory) ii) M3

  • If symptom onset is > 6h, the core must be less than 50% of the territory supplied by the occluded vessel as evident by either:

i) Hypodensity and loss of grey-white border on NCCT or ii)ADC <620 mm2/s on diffusion MRI or rCBF<30% on CTP

  • NIHSS > =8

STEP EVT INDICATION EXPANSION DOMAIN EXCLUSION CRITERIA:

  • Clinical
  • Presumed septic embolus; suspicion of bacterial endocarditis
  • Seizure at stroke onset or between onset and enrollment
  • Known anaphylactic reaction to contrast material that precludes endovascular reperfusion therapy
  • Intracranial occlusion suspected to be chronic, based on history and/or imaging
  • Intracranial dissection, based on history and/or imaging
  • Cerebral vasculitis, based on history and/or imaging
  • Known pregnancy
  • Known pre-existing medical, neurological or psychiatric disease that would confound the neurological or functional evaluations
  • Known serious, advanced, or terminal illness or life expectancy less than 6 months in the investigator judgment
  • Known or high suspicion for underlying intracranial atherosclerotic disease (ICAD)
  • Laboratory

a. Known platelet count <100,000/uL

  • Imaging
  • CT ASPECT score <6 (MRI ASPECT score <7)
  • Unfavorable vascular anatomy that limits access to the occluded artery precluding endovascular reperfusion therapy.
  • Acute occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
  • Tandem occlusions
  • Significant mass effect with midline shift (>5mm)
  • Evidence of intra-cranial tumor (except small meningioma defined as (1) <=3 cm, (2) asymptomatic) as confirmed on CT/MRI)
  • Evidence of acute intracranial hemorrhage

Treatment and study plan

Endovascular thrombectomy with any FDA-approved category POL or NRY device

Device

Endovascular thrombectomy with any FDA-approved category POL or NRY device - Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment (POL), and/or Catheter, Thrombus Retriever (NRY)

Other names: EVT, Endovascular Recanalization Therapy, Endovascular Therapy

Medical management

Other

Medical Management (MM) may involve any combination of the following: intravenous thrombolysis, antiplatelets, anti-hypertensives, cholesterol-lowering medications, and rehabilitative care.

Primary outcomes

  1. Global disability measured by Modified Rankin Score

    Time frame: 90-day

    The modified Rankin Score is a 7-outcome ordinal scale where 0 = No symptoms and 6= Dead.

    The analysis of the primary endpoint will be based on a utility weighting of the 7 outcomes, where 0 represents the worst possible health state and 1 represents the best possible state.

Other outcomes

  1. Global disability measured by Modified Rankin Score

    Time frame: 1 day of hospital discharge

    The modified Rankin Score is a 7-outcome ordinal scale where 0 = No symptoms and 6= Dead.

  2. Neurological deficit as measured by the National Institutes of Health Stroke Scale (NIHSS)

    Time frame: 24 (+/-12) hours after the time of randomization

    NIHSS is a stroke severity score that ranges from 0 to 42, with higher numbers indicating a more severe stroke.

  3. Symptomatic intracranial hemorrhage

    Time frame: 36 hours after randomization

    modified Heidelberg definition

  4. Any radiologic intracranial hemorrhage

    Time frame: 36 hours after randomization

    any acute intracranial blood, symptomatic or asymptomatic

  5. Mortality

    Time frame: 90 days

    all cause deaths

Study contacts

Contact information is provided by the study sponsor or research team.

Jordan Elm

CONTACT

[email protected]

843-876-1605

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Collaborators

  • Berry Consultants
  • MOUNT SINAI HOSPITAL
  • National Institute of Neurological Disorders and Stroke (NINDS)
  • Stony Brook University
  • The Cooper Health System
  • University at Buffalo
  • University of California, Los Angeles
  • University of Cincinnati
  • University of Pittsburgh Medical Center
  • University of Virginia

Registry information

Official study title

STEP: StrokeNet Thrombectomy Endovascular Platform

Acronym: STEP

Important dates

Study start
2025
Primary completion
2029
Study completion
2030
First posted
Mar 4, 2024
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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