NCT02767609

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

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2014

Typical duration for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2014

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

May 6, 2016

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 10, 2016

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 3, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 3, 2017

Completed
2.2 years until next milestone

Results Posted

Study results publicly available

April 30, 2019

Completed
Last Updated

April 30, 2019

Status Verified

April 1, 2019

Enrollment Period

2.8 years

First QC Date

May 6, 2016

Results QC Date

February 26, 2019

Last Update Submit

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

EXPERIMENTAL

magnetic Resonance Imaging.

Device: Magnetic Resonance Imaging

Interventions

All participants will have be given a MRI using a pseudo-continuous arterial spin labeling perfusion sequence.

Magentic Resonance Imaging

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Brain Injuries, TraumaticMultiple SclerosisAlzheimer DiseaseNeoplasms

Interventions

Magnetic Resonance Imaging

Condition Hierarchy (Ancestors)

Brain InjuriesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesCraniocerebral TraumaTrauma, Nervous SystemWounds and InjuriesDemyelinating Autoimmune Diseases, CNSAutoimmune Diseases of the Nervous SystemDemyelinating DiseasesAutoimmune DiseasesImmune System DiseasesDementiaTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental Disorders

Intervention Hierarchy (Ancestors)

TomographyDiagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Results Point of Contact

Title
Brenda Bartnik Olson
Organization
Loma Linda University medical Center

Study Officials

  • Brenda Bartnik Olson, PhD

    Loma Linda University Medical Center

    PRINCIPAL INVESTIGATOR

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