CClinicalTrials.gg
RecruitingNCT05907629CAPTIVA-MRIUpdated Jul 16, 2026

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

An observational study in Stroke and Intracranial Atherosclerotic Stenosis (ICAS), sponsored by Yale University. Recruiting at 28 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-16.

Sponsored by Yale University · Observational

From the registry’s dates

  • Started Jun 2024; still recruiting 2 years 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Stroke
  • Intracranial Atherosclerotic Stenosis (ICAS)

Browse trials for

Keywords

  • MRI
  • Stroke
  • intracranial atherosclerotic stenosis (ICAS)
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 300 is above the median of 160 across 1,692 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Yale University is the lead sponsor of 1,724 studies on the registry; 298 are open to participants now.

Of its 210 completed or terminated interventional studies of FDA-regulated products, 126 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

ICAS patients who have a recent stroke and was enrolled into CAPTIVA.

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

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
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Patient registry
No

Groups and cohorts

  • CAPTIVA-MRI Group

    CAPTIVA patients with stroke attributed to 70-99% intracranial atherosclerotic stenosis (ICAS) to aspirin plus ticagrelor, clopidogrel, or rivaroxaban.

    Other: MRI

Interventions

  • OtherMRI

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

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What researchers measure

Primary outcomes

  1. Establish ICAS hemodynamic and plaque MRI biomarkers as reliable predictors of recurrent ischemic stroke in the vascular territory of the index stroke.

    Recurrent ischemic stroke, defined as symptomatic infarct in the vascular territory of the index stroke artery. This outcome is centrally adjudicated in CAPTIVA using an American Heart Association definition of ischemic stroke

    Time frame: 12 months

07

Study locations

14 of 28 sites recruiting
  • University of Alabama Hospital
    Birmingham, Alabama 35233, United States
    • Tammy Davis · Contact · trdavis@uabmc.edu · 205-975-8572
    • Ekaterina Bakradze · Principal investigator
    Recruiting
  • University of Colorado Hospital
    Aurora, Colorado 80045, United States
    Not yet recruiting
  • Hartford Hospital
    Hartford, Connecticut 06106, United States
    Not yet recruiting
  • Yale New Haven Hospital
    New Haven, Connecticut 06510, United States
    Recruiting
  • MedStar Washington Hospital Center
    Washington D.C., District of Columbia 20010, United States
    Recruiting
  • Baptist Medical Center Jacksonville
    Jacksonville, Florida 32207, United States
    Recruiting
  • Jackson Memorial Hospital, Miami
    Miami, Florida 33136, United States
    Recruiting
  • Cleveland Clinic Tradition Hospital
    Port Saint Lucie, Florida 34987, United States
    Not yet recruiting
  • SIH Memorial Hospital of Carbondale
    Carbondale, Illinois 62901, United States
    • Jessie Henson · Contact · Jessie.henson@sih.net · 618-549-0721
    • Andrea Loggini · Principal investigator
    Not yet recruiting
  • University of Illinois Hospital
    Chicago, Illinois 60612, United States
    • Lucy Rosales · Contact · luzr@uic.edu · 312-996-2949
    • Ali Alaraj, MD · Principal investigator
    Recruiting
  • University of Chicago Medical Center
    Chicago, Illinois 60637, United States
    Recruiting
  • Metro Health Hospital
    Wyoming, Michigan 49519, United States
    Not yet recruiting
  • M Health Fairview University of Minnesota Medical Center
    Minneapolis, Minnesota 55455, United States
    Not yet recruiting
  • Barnes Jewish Hospital
    St Louis, Missouri 63108, United States
    Recruiting
  • Buffalo General Medical Center
    Buffalo, New York 14203, United States
    • Annemarie Crumlish · Contact · ac35@buffalo.edu
    • Amit Kandel · Principal investigator
    Recruiting
  • North Shore University Hospita
    Manhasset, New York 11030, United States
    Recruiting
  • NYP Columbia University Medical Center
    New York, New York 10032, United States
    Not yet recruiting
  • Carolinas Medical Center
    Charlotte, North Carolina 28203, United States
    Not yet recruiting
  • Duke University Hospital
    Durham, North Carolina 27705, United States
    Not yet recruiting
  • Cleveland Clinic Akron General
    Akron, Ohio 44307, United States
    Not yet recruiting
  • University of Cincinnati Medical Center
    Cincinnati, Ohio 45219, United States
    Recruiting
  • UH Cleveland Medical Center
    Cleveland, Ohio 44106, United States
    Recruiting
  • Mercy St. Vincent Medical Center
    Toledo, Ohio 43608, United States
    Not yet recruiting
  • Prisma Health Richland Hospital
    Columbia, South Carolina 29203, United States
    Not yet recruiting
  • University of Texas Medical Branch
    Galveston, Texas 77555, United States
    Recruiting
  • Memorial Hermann Texas Medical Center
    Houston, Texas 77030, United States
    Not yet recruiting
  • Covenant Medical Center
    Lubbock, Texas 79410, United States
    Not yet recruiting
  • UVA Medical Center
    Charlottesville, Virginia 22908, United States
    Recruiting
08

References and documents

Publications

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Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05907629
Lead sponsor
Yale University
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS)
Responsible party
Sponsor
First posted
Jun 18, 2023
Start date
Jun 24, 2024
Primary completion
Mar 31, 2029 (estimated)
Completion
Mar 31, 2029 (estimated)
Last update
Jul 16, 2026

Study contacts

Ka-Ho Wong
Contact
ka-ho.wong@hsc.utah.edu
801-585-7575
Amy Sulken
Contact
sulkenay@ucmail.uc.edu
David Liebeskind, MD
principal investigator · University of California, Los Angeles
Sepideh Amin-Hanjani, MD
principal investigator · University Hospitals
Rano Chatterjee, MD
principal investigator · Washington University School of Medicine
Adam de Havenon, MD, MS
principal investigator · Yale University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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