Cerebrovascular Reactivity Measurements With High-Density Diffuse Optical Tomography

Recruiting N/A Interventional Study
Sickle Cell Disease Cerebral Stroke
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
6 – 70
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
120 (estimated)
Sponsor
Washington University School of Medicine · Other
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About This Trial
The purpose of the study protocol is to identify imaging biomarkers for brain tissue under high metabolic stress at risk for permanent injury. We will measure oxygen extraction fraction (OEF) and cerebrovascular reactivity (CVR) in participants with and without perturbations in cerebral oxygen delivery over time to determine each parameter's role in clinical and radiologic neurologic outcomes. Mea…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 6-70 Years Old * Able to participate in MRI scan without sedation * May or may not have HbSS or beta thalassemia null genotypes of sickle cell anemia Exclusion Criteria: * Significant craniofacial malformation or technical contraindications to DOT monitoring (for HDDOT imagi…
Contacts

Kristin Guilliams, MD

3144545436

kristinguilliams@wustl.edu

CONTACT