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RECRUITINGOBSERVATIONAL

Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis- Magnetic Resonance Imaging

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

CAPTIVA-MRI is an observational multimodal MR imaging study that is ancillary to the CAPTIVA trial \[a 3-arm, double-blind Phase III trial conducted at approximately 115 StrokeNet sites randomizing patients with stroke attributed to 70-99% intracranial atherosclerotic stenosis (ICAS) to aspirin plus ticagrelor, clopidogrel, or rivaroxaban.\] The primary goal of this ancillary study is to determine if MRI biomarkers can potentially identify ICAS patients who fail best medical management. The CAPTIVA-MRI study leverages the CAPTIVA trial design and implementation to capture information that will inform and facilitate the next generation of ICAS trials and the management of patients with ICAS.

Who May Be Eligible (Plain English)

Who May Qualify: - Enrollment in the CAPTIVA trial: nondisabling symptomatic ischemic infarct stroke within 30 days secondary to 70-99% stenosis of the intracranial ICA, MCA, BA or VA - Ability to obtain baseline study MRI within 14 days of CAPTIVA enrollmen Who Should NOT Join This Trial: - Unable or unwilling to undergo MRI, including pacemaker or other MRI contraindications per American College of Radiology guidelines62 - Gadolinium contrast allergy or acute or chronic kidney disease with eGFR\<30 ml/min/1.73m2 Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Enrollment in the CAPTIVA trial: nondisabling symptomatic ischemic infarct stroke within 30 days secondary to 70-99% stenosis of the intracranial ICA, MCA, BA or VA * Ability to obtain baseline study MRI within 14 days of CAPTIVA enrollmen Exclusion Criteria: * Unable or unwilling to undergo MRI, including pacemaker or other MRI contraindications per American College of Radiology guidelines62 * Gadolinium contrast allergy or acute or chronic kidney disease with eGFR\<30 ml/min/1.73m2

Treatments Being Tested

OTHER

MRI

Additional MRI to the CAPTIVA study at baseline and 12 months follow-up

Locations (13)

University of Alabama Hospital
Birmingham, Alabama, United States
Yale New Haven Hospital
New Haven, Connecticut, United States
MedStar Washington Hospital Center
Washington D.C., District of Columbia, United States
Baptist Medical Center Jacksonville
Jacksonville, Florida, United States
Jackson Memorial Hospital, Miami
Miami, Florida, United States
SIH Memorial Hospital of Carbondale
Carbondale, Illinois, United States
University of Illinois Hospital
Chicago, Illinois, United States
University of Chicago Medical Center
Chicago, Illinois, United States
Barnes Jewish Hospital
St Louis, Missouri, United States
Buffalo General Medical Center
Buffalo, New York, United States
North Shore University Hospita
Manhasset, New York, United States
Carolinas Medical Center
Charlotte, North Carolina, United States
UH Cleveland Medical Center
Cleveland, Ohio, United States