Hyperemia detection on arterial spin labeling is associated with final infarct volume in stroke post-endovascular therapy.
Carolyn A Lomahan, Marie Luby, Georgios Kalarakis...
https://pubmed.ncbi.nlm.nih.gov/40436255Actively Recruiting
Led by National Institute of Neurological Disorders and Stroke (NINDS) · Updated on 2026-06-08
4000
Participants Needed
3
Research Sites
N/A
Total Duration
Researchers are studying stroke and related cerebrovascular diseases to better understand their natural history and develop ideas for future research. This observational study includes patients aged 18 and older who have experienced or are at risk for acute stroke or transient ischemic attacks (TIA). The study aims to establish a detailed registry with clinical, laboratory, and imaging data to explore relationships among disease characteristics and outcomes. Participants undergo standard medical care tests such as blood and urine analyses, EKG, CT scans, MRI, Transcranial Doppler, and echocardiograms. Some tests may be repeated at follow-up visits scheduled at 1, 3, and 12 months to observe changes over time. Research-specific blood and urine samples are also collected to assess biomarkers and gene expression related to stroke. Throughout the study, participants will be monitored with imaging studies to identify abnormalities linked to stroke severity and progression. Clinical assessments include stroke severity scales and functional outcome measures. Data collection also involves evaluating gene expression and biomarkers from blood samples. The total participation time can extend up to a year with multiple follow-up assessments to track recovery and disease progression.
CONDITIONS
Natural History of Stroke: Cause and Development
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within 30 days post-acute event
Participants undergo neuroimaging and clinical assessments to evaluate cerebrovascular abnormalities and stroke severity.
Visits at post-acute, 24 hours, 5 days or discharge, and 30 days
Duration - Up to 12 months
Participants are monitored over time to assess clinical outcomes, biomarker levels, and stroke recovery.
Visits at 3 months, 6 months, and 12 months
Total: 3 locations
1
Medstar Washington Hospital Center
Washington D.C., District of Columbia, United States, 20010
Actively Recruiting
2
Suburban Hospital - Johns Hopkins Medicine
Bethesda, Maryland, United States, 20814
Actively Recruiting
3
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
N
Nicole L Peterkin
L
Lawrence L Latour, Ph.D.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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