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.
SUMMIT RISE Study of Acute Ischemic Stroke Patients
At a glance
Conditions
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.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Periprocedural eTICI measurement of revascularizationPeriprocedural
Revascularization status checklist