About this trial
This prospective, randomized controlled trial will compare two manual aspiration techniques for treating acute ischemic stroke due to large vessel occlusion: cyclic aspiration (Plunger technique) and static aspiration. Both techniques use FDA-approved devices (Raptor Aspiration Catheters and VacLok syringes) and are standard of care. Approximately 500 participants across 20 sites will be randomized to one of the two techniques. The primary endpoint is First Pass Effect (TICI 2c/3 after first attempt), with secondary endpoints including overall recanalization and 90-day functional outcomes. Results will address a critical gap in optimizing aspiration thrombectomy techniques.
Eligibility criteria
Qualifiers
None
Disqualifiers
Evidence of acute intracranial hemorrhage prior to treatment, Failure to obtain informed consent
Trial design
Treatments tested in this trial
- Plunger Technique
- Static Manual Aspiration Thrombectomy
Treatment groups
Locations
Sponsors and collaborators
Vanderbilt University Medical Center
Lead sponsor
Balt USA
Collaborator