Condition: Acute Ischemic Stroke · Sponsor: RapidPulse, Inc
The goal of this clinical trials is to demonstrate the safety and effectiveness for the RapidPulseTM Aspiration System in patients experiencing acute ischemic stroke within 8 hours of symptom onset or last seen normal. Subjects will undergo mechanical thrombectomy (a procedure to remove a clot in the brain which is preventing blood flow), with the RapidPulseTM Aspiration System. Participation in the trial is for 90 days.
This description comes directly from the study's public registry record.
Cynthia Yang · 9498367402 · cyang@rapidpulsemed.com
Always discuss trial participation with your own doctor first.
| Providence Saint John's Medical Foundation | Torrance, California, United States | Recruiting |
| Yale University | New Haven, Connecticut, United States | Not Yet Recruiting |
| Baptist Health Research Institute | Jacksonville, Florida, United States | Recruiting |
| University of South Florida | Tampa, Florida, United States | Recruiting |
| Emory University at Grady | Atlanta, Georgia, United States | Recruiting |
| Rush University Medical Center | Chicago, Illinois, United States | Recruiting |
| Advocate Aurora Research Institute | Park Ridge, Illinois, United States | Not Yet Recruiting |
| Indiana University Health | Indianapolis, Indiana, United States | Not Yet Recruiting |
| State University of Iowa | Iowa City, Iowa, United States | Not Yet Recruiting |
| Washington University | St Louis, Missouri, United States | Not Yet Recruiting |
| Cooper Health System | Camden, New Jersey, United States | Not Yet Recruiting |
| State University of New York at Buffalo | Buffalo, New York, United States | Recruiting |
+ 18 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06029491