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Clinical Trials/NCT04099823
NCT04099823
Recruiting
Not Applicable

MR Evaluation of Cerebrospinal Fluid (CSF) Dynamics and Association of Intracranial CSF Flow With Brain Function

Mayo Clinic2 sites in 1 country50 target enrollmentOctober 31, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hydrocephalus
Sponsor
Mayo Clinic
Enrollment
50
Locations
2
Primary Endpoint
CSF flow measurement
Status
Recruiting
Last Updated
3 months ago

Overview

Brief Summary

The Researchers are trying to test a MR imaging method for detection of Cerebral Spinal Fluid (CSF) flow in the brain to help diagnosis and better understand diseases that affect brain function.

Detailed Description

The purpose of this research is to figure out if MR imaging can detect movement of CSF (fluid around the brain) to help better diagnosis and understand the cause of diseases that affect brain function. We are doing this research study to find out if movement of CSF is different between healthy adults and those with a disease that affects brain function.

Registry
clinicaltrials.gov
Start Date
October 31, 2019
End Date
January 1, 2027
Last Updated
3 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Petrice M. Cogswell

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • A healthy control 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.
  • Patients who have a suspected diagnosis of altered CSF dynamics including but not limited to normal pressure hydrocephalus will be referred to Dr. Cogswell by their care team to be included in the study. Conditions of altered CSF dynamics include obstructive and non-obstructive hydrocephalus and may be associated with headaches and/or decreased cognitive function.
  • Similarly, patients with impaired cognitive function including but not limited to Alzheimer's disease will be referred to Dr. Cogswell by their care team to be included in the study.

Exclusion Criteria

  • Subjects with non-MRI compatible devices
  • required sedation
  • women who may be pregnant will be excluded.
  • The first 10 subjects with normal pressure hydrocephalus will not have previously been shunted.

Outcomes

Primary Outcomes

CSF flow measurement

Time Frame: At the time of MR exam, approximately one hour

CSF flow will be measured in participants and compared between those with unimpaired brain function and those with clinical diagnosis of a disease that affects brain function, such as Alzheimer's disease and normal pressure hydrocephalus.

Secondary Outcomes

  • White matter disease(At the time of MR exam, approximately one hour)
  • Volume of CSF spaces(At the time of MR exam, approximately one hour)

Study Sites (2)

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