Measuring Cerebral Blood Flow Using Pseudo-continuous Arterial Spin Labeling Perfusion Magnetic Resonance Imaging
1 other identifier
interventional
1
0 countries
N/A
Brief Summary
This study will test a new MRI sequence that measures cerebral blood flow (CBF). Because this technique for measuring CBF is new, there is little information on what the normal values for different regions of the brain should be. Information from the study will be used to establish normative CBF values for the brain, improving the reliable use of this technique for the diagnosis of brain injury or disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2014
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2014
CompletedFirst Submitted
Initial submission to the registry
May 6, 2016
CompletedFirst Posted
Study publicly available on registry
May 10, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 3, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 3, 2017
CompletedResults Posted
Study results publicly available
April 30, 2019
CompletedApril 30, 2019
April 1, 2019
2.8 years
May 6, 2016
February 26, 2019
April 9, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Regional Cerebral Blood Flow Values of the Brain Measured Using Pseudo-continuous Arterial Spin Labeling (pCASL) MRI.
The relative cerebral blood flow (CBF) in frontal, parietal, occipital gray matter and white matter regions, basal ganglia, thalami, and cerebellum will be measured using region of interest analysis to determine institutional normative values for healthy subjects.
single encounter
Study Arms (1)
Magentic Resonance Imaging
EXPERIMENTALmagnetic Resonance Imaging.
Interventions
All participants will have be given a MRI using a pseudo-continuous arterial spin labeling perfusion sequence.
Eligibility Criteria
You may qualify if:
- Any person between the ages of 18-90 years, who is undergoing routine magnetic resonance imaging (MRI) of the head with or without contrast at Loma Linda University Medical Center.
- Must be eligible for MRI (no electronic or metal implants that are not MR compatible).
You may not qualify if:
- Electronic or metal implant that is not MRI safe, pregnancy or claustrophobia.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Brenda Bartnik Olson
- Organization
- Loma Linda University medical Center
Study Officials
- PRINCIPAL INVESTIGATOR
Brenda Bartnik Olson, PhD
Loma Linda University Medical Center
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Proffesor
Study Record Dates
First Submitted
May 6, 2016
First Posted
May 10, 2016
Study Start
May 1, 2014
Primary Completion
March 3, 2017
Study Completion
March 3, 2017
Last Updated
April 30, 2019
Results First Posted
April 30, 2019
Record last verified: 2019-04
Data Sharing
- IPD Sharing
- Will not share