Actively Recruiting

Age: 45Years - 90Years
All Genders
NCT06116630

StrokeCog-BBB to Study Cognitive Outcomes Following Stroke

Led by Stanford University · Updated on 2024-04-18

350

Participants Needed

1

Research Sites

293 weeks

Total Duration

On this page

Sponsors

S

Stanford University

Lead Sponsor

U

University of Manchester

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to learn about cognitive outcomes in stroke patients. The main question it aims to answer are: 1. Is blood-brain barrier permeability compromised for years after stroke, 2. Is a blood biomarker of imbalanced angiogenesis dysregulated in chronic stroke and 3. Are there biomarkers that separately or together predicts cognitive decline after stroke, and are other MRI, blood, and clinical characteristics that are associated. Participants will undergo cognitive testing and MRIs two years apart. Researchers will compare cognitive outcomes in non-stroke patients who have cardiovascular risk factors to understand the effects of stroke on these outcomes.

CONDITIONS

Official Title

StrokeCog-BBB to Study Cognitive Outcomes Following Stroke

Who Can Participate

Age: 45Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 45 years or over
  • Have one or more vascular risk factors such as high blood pressure, diabetes, or vascular disease like angina, previous heart attack, heart bypass, or peripheral artery disease
  • Established vascular disease (previous myocardial infarction, angina, or vascular stent in peripheral arteries)
  • Sufficiently fluent in written and spoken English
  • Living independently in the community
  • Willing and able to give consent to participate in the study
Not Eligible

You will not qualify if you...

  • Currently treated with IL-1 blockade or immune-suppressant therapy, or treated within the last 3 months
  • Currently participating in a clinical trial of investigational medicinal product or device trial
  • No history of previous ischemic or hemorrhagic stroke, mini-stroke, or serious brain injury
  • Diagnosed with dementia
  • Have renovascular disease
  • Have major neurological disease such as immune-mediated disorders or previous brain tumors

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Stanford University Hospital

Palo Alto, California, United States, 94304

Actively Recruiting

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Research Team

M

Muhith Musabbir

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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