Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
130

Summary

Conditions
  • Anemia
  • Healthy Controls
  • Iron Deficiency Anemia
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 16 years and 60 years
Gender
Both males and females

Description

This is an observational trial, in patients with moderate to severe anemia and control subjects. The main purpose of this study is to understand whether normal brain blood flow, oxygen extraction reserve, white matter volumes, and brain functional connectivity are affected by acquired anemia. The in...

This is an observational trial, in patients with moderate to severe anemia and control subjects. The main purpose of this study is to understand whether normal brain blood flow, oxygen extraction reserve, white matter volumes, and brain functional connectivity are affected by acquired anemia. The investigators will perform baseline MRI monitoring for all subjects. All eligible subjects will be asked to provide informed consent before participating in the study. Comprehensive cerebrovascular MRI, baseline bloodwork, and neurocognitive testing will be collected from all subjects.

Tracking Information

NCT #
NCT04320966
Collaborators
Not Provided
Investigators
Principal Investigator: John Wood, MD,PhD Children's Hospital Los Angeles