NCT07115940 Medical Management With Endovascular Thrombectomy Versus Medical Management Alone in Patients Presenting Beyond 24 Hours of Last Known Well
| NCT ID | NCT07115940 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Amrou Sarraj |
| Condition | Acute Ischemic Stroke |
| Study Type | INTERVENTIONAL |
| Enrollment | 408 participants |
| Start Date | 2026-05-01 |
| Primary Completion | 2029-11-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 408 participants in total. It began in 2026-05-01 with a primary completion date of 2029-11-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
SELECT LATE trial aims to evaluate if addition of endovascular thrombectomy to medical management in patients presenting with acute ischemic stroke and a proximal large vessel occlusion in the anterior circulation between 24 and 72 hours of stroke onset results in achieving better functional outcomes (measured using modified Rankin Scale Scores) at 90-day follow-up (± 15 days).
Eligibility Criteria
Inclusion Criteria: General Inclusion Criteria: * Adults (18-85\* years) with the final diagnosis of an acute ischemic stroke$ * NIHSS ≥ 6 * Time from last-known-well to randomization \>24 - 72 hours * Pre-stroke modified Rankin Scale score of 0-1 * Eligible for thrombectomy and medical management * Signed Informed Consent obtained * Subject willing to comply with the protocol follow-up requirements * Anticipated life expectancy of at least 3 months \*Inclusive of both 18 and 85 years of age (i.e. up to 86th birthdate). $Subacute presentation - In-hospital stroke admissions with fluctuating clinical symptoms for patients who presented to EVT centers within 24 hours of when they were last known well will not be eligible for the trial. General Exclusion Criteria * Current participation in another investigational interventional drug or device study. * Baseline Platelet count \<100,000/μl Imaging Inclusion Criteria * Proven large vessel occlusion in ICA or MCA-M1 occlusion (carotid occlusions can be cervical or intracranial, with or without tandem MCA lesions), as determined by MR Angiography (MRA) or CT Angiography (CTA) * CT ASPECTS 3-10 * CT Perfusion ischemic core (rCBF \<30%)# volume ≤150 ml OR MR Diffusion ischemic core (ADC \<620x10-6 mm2/s)# volume ≤150ml #If the perfusion software at enrollment center uses another threshold/measure to define ischemic core, please use that measure to assess ischemic core criteria. Imaging Exclusion Criteria * Evidence of intracranial tumor (except small meningioma \<3cm without signs of edema or inflammation), acute intracranial hemorrhage, or arteriovenous malformation * Significant mass effect, defined as midline shift (\>3mm) using foramen of monroe (anterior margin of third ventricle) as the marker for midline instead of septum pellucidum AND/OR Effacement of sulci in contralateral hemisphere * Evidence of internal carotid artery dissection that is flow limiting or aortic dissection * Intracranial stent implanted in the same vascular territory that precludes the safe deployment/removal of the neurothrombectomy device * 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). * Any signs of established infarct, demarcating hypodensity and area of cerebral edema on non-contrast CT * CT ASPECTS 0-2 * CT Perfusion ischemic core (rCBF \<30%)# volume \>150 ml OR MR Diffusion ischemic core (ADC \<620x10-6 mm2/s)# volume \>150ml #If the perfusion software at enrollment center uses another threshold/measure to define ischemic core, please use that measure to assess ischemic core criteria.
Contact & Investigator
Amrou Sarraj, MD
PRINCIPAL INVESTIGATOR
University Hospitals
Frequently Asked Questions
Who can join the NCT07115940 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 85 Years, studying Acute Ischemic Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07115940 currently recruiting?
Yes, NCT07115940 is actively recruiting participants. Contact the research team at Kathryn.Rownd@UHhospitals.org for enrollment information.
Where is the NCT07115940 trial being conducted?
This trial is being conducted at Chicago, United States, Kansas City, United States, St Louis, United States, Providence, United States and 2 additional locations.
Who is sponsoring the NCT07115940 clinical trial?
NCT07115940 is sponsored by Amrou Sarraj. The principal investigator is Amrou Sarraj, MD at University Hospitals. The trial plans to enroll 408 participants.
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