A Study to Compare CSF Flow Metrics Across Platforms
Comparison of CSF Flow Metrics Across MRI Platforms
1 other identifier
observational
10
1 country
1
Brief Summary
The purpose of this research is to find out more about detecting movement of CSF (fluid around the brain) with MRI. Researchers are doing this research study to find out how measurements of CSF movement differ among MRI machines and how image quality is changed by reducing the scan time.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Sep 2022
Shorter than P25 for all trials
1 active site
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
First Submitted
Initial submission to the registry
January 23, 2022
CompletedFirst Posted
Study publicly available on registry
February 3, 2022
CompletedStudy Start
First participant enrolled
September 14, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 20, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 20, 2023
CompletedSeptember 19, 2024
September 1, 2024
5 months
January 23, 2022
September 16, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Comparison of flow metrics among scanners
Flow metrics such as average total flow will be compared among multiple MRI scanners
February -December 2022
Comparison of flow metrics between scans with and without parallel imaging
Flow metrics such as the average total flow will be compared between sequences acquired with and without acceleration techniques, including parallel imaging, for a given scanner
February -December 2022
Eligibility Criteria
The study population will include healthy young adults, ages 18-40 years.
You may qualify if:
- \- A healthy volunteer will be defined as an otherwise healthy person who does not have a medical condition that affects brain function or have problems with concentration, memory, balance, or coordination.
You may not qualify if:
- \- Subjects with non-MRI compatible devices, required sedation (claustrophobia or unable to remain still for exam), or women who are pregnant will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mayo Cliniclead
Study Sites (1)
Mayo Clinic
Rochester, Minnesota, 55905, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Petrice Cogswell, MD, PhD
Mayo Clinic
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 23, 2022
First Posted
February 3, 2022
Study Start
September 14, 2022
Primary Completion
February 20, 2023
Study Completion
February 20, 2023
Last Updated
September 19, 2024
Record last verified: 2024-09