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Search / Trial NCT05907629

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

Launched by YALE UNIVERSITY · Jun 7, 2023

Trial Information

Current as of August 20, 2025

Recruiting

Keywords

Mri Stroke Intracranial Atherosclerotic Stenosis (Icas)

ClinConnect Summary

The CAPTIVA-MRI clinical trial is studying the best ways to treat patients who have had a stroke due to narrowing of the blood vessels in the brain, specifically looking at a condition called intracranial atherosclerotic stenosis (ICAS). The main goal is to see if special MRI scans can help identify patients who are not responding well to standard treatments. This study is part of a larger trial that compares different blood-thinning medications to find the most effective one for preventing future strokes.

To be eligible for this trial, participants must have experienced a mild stroke within the last 30 days due to significant narrowing of certain brain arteries. They also need to be able to have an MRI scan within two weeks of joining the main trial. Those with certain medical conditions that prevent them from having an MRI or who are allergic to the contrast dye used in some scans may not qualify. If you participate, you can expect to have an MRI as part of the study, which will help researchers understand how to better manage and treat patients with this condition in the future.

Gender

ALL

Eligibility criteria

  • 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

About Yale University

Yale University, a prestigious Ivy League institution located in New Haven, Connecticut, is renowned for its commitment to advancing medical research and clinical innovation. With a rich history of academic excellence and a robust infrastructure for scientific inquiry, Yale serves as a leading sponsor for clinical trials aimed at improving patient care and developing new therapeutic approaches. The university's multidisciplinary teams of researchers and clinicians collaborate to conduct rigorous and ethical studies, leveraging cutting-edge technologies and methodologies to address critical health challenges. Through its dedication to fostering an environment of inquiry and discovery, Yale University plays a pivotal role in translating research findings into clinical practice, ultimately enhancing health outcomes for diverse populations.

Locations

Washington, District Of Columbia, United States

Charlotte, North Carolina, United States

Chicago, Illinois, United States

Buffalo, New York, United States

New Haven, Connecticut, United States

Chicago, Illinois, United States

Jacksonville, Florida, United States

Saint Louis, Missouri, United States

Birmingham, Alabama, United States

Cleveland, Ohio, United States

Miami, Florida, United States

Manhasset, New York, United States

Carbondale, Illinois, United States

Patients applied

0 patients applied

Trial Officials

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

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported