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Study identifier: NCT05611242 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Proximal Internal Carotid Artery Acute Stroke Secondary to Tandem or Local Occlusion Thrombectomy Trial

Condition: Acute Ischemic Stroke  ·  Sponsor: Mercy Health Ohio

PhasePhase 3
Planned participants404
Who can joinAll sexes, 18 Years to 79 Years
Healthy volunteersNo

About this study

The primary objective is to establish the efficacy of intra-arterial (IA) mechanical thrombectomy (MT) with extracranial proximal carotid artery acute stenting versus non-stenting approaches in patients with acute ischemic stroke (AIS) from intracranial vessel occlusion (IVO) in the anterior circulation and have a proximal carotid occlusive disease (occlusion or severe stenosis).

This description comes directly from the study's public registry record.

Talk to the study team

Jasmine M Olvany, PhD  ·  (419)-251-4264  ·  jolvany@mercy.com

Laila Ibrahim, MPH  ·  librahim@mercy.com

Always discuss trial participation with your own doctor first.

Locations (51)

Mobile Infirmary Medical CenterMobile, Alabama, United StatesRecruiting
Glendale Adventist Medical CenterGlendale, California, United StatesRecruiting
University of California, IrvineIrvine, California, United StatesRecruiting
Pomona ValleyPomona, California, United StatesRecruiting
Sutter Institute for Medical ResearchSacramento, California, United StatesNot Yet Recruiting
California Pacific Medical Center/Mils Peninsula Medical CenterSan Francisco, California, United StatesRecruiting
Boca Raton - Baptist HealthBoca Raton, Florida, United StatesRecruiting
Delray Medical CenterDelray Beach, Florida, United StatesRecruiting
Baptist Health Research InstituteJacksonville, Florida, United StatesRecruiting
University of Florida Health JacksonvilleJacksonville, Florida, United StatesRecruiting
University of Miami School of MedicineMiami, Florida, United StatesRecruiting
Orlando Health, Inc.Orlando, Florida, United StatesRecruiting

+ 39 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05611242