Endovascular Therapy for Large Core Patients With Uncertain Response to Thrombectomy
Launched by STANFORD UNIVERSITY · Apr 29, 2025
Trial Information
Current as of June 26, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
This is a pilot prospective randomized trial of patients with acute ischemic anterior circulation strokes due to large artery occlusion who present with an eligible large ischemic core lesion, and who can be treated within 24 hours of stroke onset. The results of this pilot study will be used as preliminary data for a larger NIH-funded multi-center randomized trial to address the knowledge gaps in the management of this patient population.
Eligible patients will be randomized 1:1 to either:
Endovascular therapy plus medical therapy (based on current AHA guidelines)
or
Medical therapy (b...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Signs and symptoms consistent with an acute anterior circulation ischemic stroke and associated brain imaging
- • 2. Baseline NIHSSS is ≥10 and remains ≥10 immediately prior to randomization
- • 3. Treatment can be initiated within 24 hours of stroke onset or time last known well and within 120 minutes of completion of qualifying imaging
- • 4. Functionally independent prior to stroke onset
- • 5. Patient/ Legally Authorized Representative has signed the Informed Consent form.
- Exclusion Criteria:
- • 1. Other serious, advanced, or terminal illness (investigator judgment) or life expectancy is less than 6 months.
- • 2. Pre-existing medical, neurological or psychiatric disease that would confound the neurological or functional evaluations
- • 3. Pregnant
- • 4. Unable to undergo a contrast brain perfusion scan with either MRI or CT
- • 5. Known allergy to iodine that precludes an endovascular procedure
- • 6. Treated with tPA or TNK \>4.5 hours after time last known well
- • 7. Seizures at stroke onset if it precludes obtaining an accurate baseline NIHSS
- • 8. Baseline blood glucose of \<50mg/dL (2.78 mmol) or \>400mg/dL (22.20 mmol)
- • 9. Baseline platelet count \< 50,000/uL
- • 10. Severe, sustained hypertension (SBP \>185 mmHg or DBP \>110 mmHg)
- • 11. Current participation in another investigational drug or device study
- • 12. Presumed septic embolus; suspicion of bacterial endocarditis
- • 13. Any other condition that, in the opinion of the investigator, precludes an endovascular procedure or poses a significant hazard to the subject if an endovascular procedure was performed.
- NEUROIMAGING Exclusion:
- • 1. Evidence of intracranial tumor (except small meningioma) acute intracranial hemorrhage, neoplasm, or arteriovenous malformation
- • 2. Significant mass effect with midline shift
- • 3. Evidence of internal carotid artery dissection that is flow limiting or aortic dissection
- • 4. Intracranial stent implanted in the same vascular territory that precludes the safe deployment/removal of the neurothrombectomy device
- • 5. Acute symptomatic arterial occlusions in more than one vascular territory confirmed on CTA/MRA (e.g., bilateral MCA occlusions, or an MCA and a basilar artery occlusion).
About Stanford University
Stanford University is a prestigious academic institution renowned for its cutting-edge research and innovation in healthcare and medicine. As a clinical trial sponsor, Stanford leverages its extensive resources, including a collaborative network of world-class researchers and state-of-the-art facilities, to advance medical knowledge and improve patient care. The university is committed to conducting rigorous, ethical research that adheres to the highest standards of scientific integrity, fostering an environment where groundbreaking discoveries can translate into effective clinical applications. Through its clinical trials, Stanford aims to address critical health challenges and contribute to the development of novel therapies and treatment strategies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Palo Alto, California, United States
Patients applied
Trial Officials
Gregory Albers, MD
Principal Investigator
Stanford University
Jeremy Heit, MD
Principal Investigator
Stanford University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported