Actively Recruiting

Age: 30Years +
All Genders
Healthy Volunteers
ID05518305

Platelet Expression of Fcb3RIIa and Arterial Hemodynamics to Predict Recurrent Stroke in Intracranial Atherosclerosis

Led by University of California, Los Angeles · Updated on 2025-04-16

250

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

U

University of Pittsburgh Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to find out if people with higher levels of platelet Fcb3RIIa have a greater risk of having another ischemic stroke. It focuses on patients who have had a minor stroke or transient ischemic attack (TIA) caused by intracranial atherosclerotic disease (ICAD). Researchers want to understand how blood flow changes and platelet activity contribute to stroke recurrence by using imaging and blood tests. Participants will undergo blood sampling and magnetic resonance imaging (MRI) along with standard stroke cognitive tests when they join the study. They will have a follow-up visit after three months to check for any adverse events and repeat cognitive tests. After 12 months, another MRI and cognitive test will be done to evaluate their condition. Throughout the study, researchers will measure platelet Fcb3RIIa expression and wall shear stress from CT angiography using computational fluid dynamics. These measurements will help predict the risk of recurrent stroke over one year. Participants will be monitored with imaging and cognitive assessments to track any silent or clinical strokes, helping to develop a personalized risk model for stroke recurrence.

CONDITIONS

Brief Title

Platelet Expression of FcγRIIa and Arterial Hemodynamics to Predict Recurrent Stroke in Intracranial Atherosclerosis

Who Can Participate

Age: 30Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Stroke with symptoms lasting more than 24 hours and imaging evidence of acute ischemia in the affected vessel territory
  • Minor stroke defined as NIHSS score less than 6
  • Eligible transient ischemic attack (TIA) with specific imaging abnormalities or multiple stereotyped ischemic events
  • Intracranial atherosclerotic disease affecting intracranial carotid, middle cerebral, vertebral, or basilar arteries
  • Stenosis of 50-99% measured by CTA using WASID criteria
  • Age 30 or older; ages 30-49 require established atherosclerotic disease elsewhere or two or more risk factors
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Stroke or TIA caused by other known conditions such as atrial fibrillation, mitral stenosis, mechanical valve, intracardiac thrombus, dilated cardiomyopathy, or proximal carotid/vertebral stenosis over 50%
  • Contraindications to MRI including incompatible metallic implants or electronic devices
  • Pregnancy or breastfeeding
  • Morbid obesity or severe claustrophobia preventing MRI
  • Other causes of stroke or TIA not related to intracranial atherosclerosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - At enrollment

Participants undergo blood sampling, magnetic resonance imaging (MRI), and stroke cognitive tests to collect baseline data related to their stroke and intracranial atherosclerotic disease.

1 visit (in-person)

Monitoring

Duration - 3 months after enrollment

Participants are monitored for adverse events and undergo a follow-up cognitive stroke test to assess their condition and recovery progress.

1 visit (in-person)

Diagnostic Evaluation

Duration - 12 months after enrollment

Participants undergo a follow-up MRI and cognitive stroke test to evaluate for recurrent silent ischemia and stroke at 12 months.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Ronald Reagan UCLA Medical Center

Los Angeles, California, United States, 90095

Actively Recruiting

Loading map...

Research Team

D

David Liebeskind, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Similar Trials

18F FDG and 68Ga FAPI PET/MR Imaging of Carotid Artery Plaqu...

Carotid Artery Plaque

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here