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A Randomized, Controlled Trial to Evaluate the Safety and Effectiveness of the Route 92 Medical Reperfusion System (SUMMIT MAX)

Completed · Not applicable · NCT05018650

Conditions: Acute Ischemic Stroke

At a glance

Research payments reported, 2025
$271,422
U.S. investigators named
17
Sites paid
17
Planned or actual enrollment
250

About the trial

Sponsor
Route 92 Medical, Inc.
Tested
Route 92 Medical Reperfusion System (device)
Dates
Started 2021-12-21; completion 2024-05-22
Results posted
Not yet

The SUMMIT MAX study is a prospective, randomized, controlled, interventional clinical trial to evaluate the safety and effectiveness of the Route 92 Medical MonoPoint® Reperfusion System with the Hi Point 88 and HiPoint 70 Reperfusion Catheters for aspiration thrombectomy in acute ischemic stroke patients.

From ClinicalTrials.gov, last updated 2025-04-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Route 92 Medical, Inc. reported $271,422 in research payments for this study in 2025 (20 payments).

Products named: 088 Access System, Hipoint 088, Nipoint 088

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.