Thrombectomy Clinical Trials

Clinical trials related to Thrombectomy Procedure

Medical Management With Endovascular Thrombectomy Versus Medical Management Alone in Patients Presenting Beyond 24 Hours of Last Known Well - SELECT LATE Trial

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• 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.

Locations
United States
Illinois
University of Chicago
RECRUITING
Chicago
Kansas
The University of Kansas Health System
RECRUITING
Kansas City
Missouri
Washington University School of Medicine
RECRUITING
St Louis
Rhode Island
Rhode Island Hospital
RECRUITING
Providence
Texas
Baylor University Medical Center
RECRUITING
Dallas
West Virginia
West Virginia University
RECRUITING
Morgantown
Contact Information
Primary
Kate Rownd, MED
Kathryn.Rownd@UHhospitals.org
216-286-6458
Backup
Deep Pujara, MBBS, MPH, MS
Deep.Pujara@UHHospitals.org
Time Frame
Start Date: 2026-05-01
Estimated Completion Date: 2029-12-01
Participants
Target number of participants: 408
Treatments
Experimental: Medical Management with Endovascular Thrombectomy
Medical management with endovascular thrombectomy (EVT) - EVT will be provided in addition to medical management and is a procedure to remove a thrombus in one of the brain arteries that is obstructing the blood flow. Removing this occlusion results in restoration of blood flow to ischemic brain tissue and salvage of the parts that are still viable, which is expected to improve functional outcomes. Endovascular thrombectomy procedure will be performed using stent retrievers, aspiration devices or combination approach at the discretion of the treating physician, using devices approved by the local regulatory authority. For patients treated in the United States of America, only US Food and Drug Administration-approved neurothrombectomy devices can be used.
Active_comparator: Medical Management without Endovascular Thrombectomy
Medical management without endovascular thrombectomy comprises various measures to prevent further deterioration, enhance patients' outcomes and prevent occurrence of a secondary stroke in short and long term. This includes 1) evidence-based practices for blood pressure management 2) Neurocritical care monitoring with appropriate osmotic therapy and neurosurgical interventions such as hemicraniectomy for management of cerebral edema that occurs due to infracted brain tissue based on local institutional protocol, 3) stroke etiology identification by requisite neurology , cardiology, immunology evaluations and 4) short and long-term strategies for secondary stroke prevention, including anticoagulation, antiplatelet therapy, medical optimization and modification of stroke risk factors such as hypertension, hyperlipidemia, diabetes and other potential comorbidities.
Sponsors
Leads: Amrou Sarraj
Collaborators: Patient-Centered Outcomes Research Institute

This content was sourced from clinicaltrials.gov