SUMMIT RISE Study for Acute Ischemic Stroke

This study, called SUMMIT RISE, is looking at how well a device called the Route 92 Medical Reperfusion Systems works for people who have had an acute ischemic stroke (a stroke caused by a blood clot blocking blood flow to the brain). The device is used during a procedure called mechanical thrombectomy, which removes the clot. The study wants to see how well the device reopens blood vessels during the procedure. You might be able to join if you are at least 18 years old, had an acute ischemic stroke, and were treated with the Route 92 Medical Reperfusion System within 8 hours of when your stroke symptoms started. The study aims to enroll 500 participants.

Study design
This interventional study plans to enroll 500 participants. It is evaluating a medical device for acute ischemic stroke patients.
What's involved
You would need to provide informed consent within 72 hours after your thrombectomy procedure.
Compensation
Not stated in the trial record.
Follow-up
The primary outcome of blood vessel reopening is measured during the procedure.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07436156

SUMMIT RISE Study of Acute Ischemic Stroke Patients

Recruiting
PHASE4Ages 18+InterventionalTreatment
Route 92 Medical, Inc.
~500 participants
Updated 2026-02-27 on ClinicalTrials.gov
What's tested:Route 92 Medical Reperfusion Systems

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Periprocedural eTICI measurement of revascularization
Measured over Periprocedural
Acute Ischemic Stroke

NCT07436156

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Route 92 Medical, Inc.

    West Jordan, Utahstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Renee Kochevar Vice President, Clinical Research, PhD, ALM
Email the study team

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Eligibility criteria

Inclusion

Acute ischemic stroke patient initially treated (first pass) with a Route 92 Medical Reperfusion System
Informed consent completed and documented within 72 hours following thrombectomy procedure
Endovascular treatment initiated (defined as time of groin puncture) within 8 hours from time last known well
Age ≥ 18 years

Exclusion

None
  • Periprocedural eTICI measurement of revascularizationPeriprocedural

    Revascularization status checklist