Actively Recruiting
Individual Cerebral Hemodynamic Oxygenation Relationships (ICHOR 1) Observational Study in Pediatric Patients Requiring Clinical Anesthesia for MRI
Led by Children's Hospital Los Angeles · Updated on 2026-04-29
1000
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
Sponsors
C
Children's Hospital Los Angeles
Lead Sponsor
N
National Heart, Lung, and Blood Institute (NHLBI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This observational study focuses on patients who require clinical anesthesia for an MRI scan, aiming to understand how different anesthesia types affect cerebral blood flow and oxygen metabolism. It includes children from birth up to 18 years old who need a clinical MRI and for whom anesthetic choice is undecided. The study is sponsored by Children's Hospital Los Angeles and seeks to gather important data on brain hemodynamics under anesthesia. Participants who qualify and provide consent will have their standard clinical MRI extended by up to 7.5 minutes on up to five occasions to acquire additional images related to cerebral blood flow and venous oxygenation. Standard anesthesia care, safety monitoring, and dosing will remain unchanged throughout the MRI procedure. After the MRI, non-invasive hematocrit monitoring will also be performed. During the study, participants will undergo the extended MRI scans in a standard clinical environment with full clinical oversight for safety during anesthesia induction, maintenance, and recovery. Researchers will collect structural and metabolic MRI data, focusing on changes in cerebral blood flow and oxygen metabolism over about 60 minutes from the start to the end of the MRI. The total involvement duration depends on the MRI schedule and clinical care.
CONDITIONS
Brief Title
Individual Cerebral Hemodynamic Oxygenation Relationships (ICHOR 1)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to tolerate an MRI
- Scheduled for a clinically indicated MRI
- Between birth and up to 18 years old
You will not qualify if you...
- Presence of MRI-incompatible device or implant (e.g., pacemakers, stents)
- Unable to tolerate enclosed spaces and loud noises during MRI
- Preterm infants less than 25 weeks
- Clinically too unstable to have MRI extended by up to 7.5 minutes
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 day
Participants undergo clinical MRI with extended imaging up to 7.5 minutes to assess cerebral blood flow and oxygen metabolism while receiving standard-of-care anesthesia.
Up to 5 MRI sessions
Duration - Immediate post-MRI period
Participants have non-invasive hematocrit monitoring immediately following each MRI exam to support safety assessments.
Up to 5 monitoring sessions following MRI
Trial Site Locations
Total: 1 location
1
Children's Hospital Los Angeles
Los Angeles, California, United States, 90027
Actively Recruiting
Research Team
H
Hannah E Wiseman, MPH
M
Matthew T Borzage, PhD
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
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