Evaluation Of Brain Glymphatic Kinetics Following Intrathecal Administration Of Gadolinium In Healthy Adult Volunteers
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Healthy
- Sponsor
- Weill Medical College of Cornell University
- Enrollment
- 19
- Locations
- 1
- Primary Endpoint
- Drug distribution over time
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This study is being done in order to see how gadolinium-based MRI contrast (Magnevist) travels through the central nervous system (CNS) when injected through the spinal column, and to compare differences between two age groups (age 20-50, and 51-80). This will allow investigators to evaluate how much contrast has crossed into the tissue surrounding the brain. Such information will help investigators determine whether this kind of contrast can be used to model how other drugs might travel through the CNS and evaluate its use as an illustrative imaging marker that mirrors the glymphatic system.
Detailed Description
This is a prospective, longitudinal study of MR imaging of intrathecally delivered gadolinium contrast (Magnevist, Gd-DTPA) in healthy adult male and female subjects. Subjects will be divided into two groups (20-50 years old and 51-80 years old) both of which will receive intrathecal injection of the drug Magnevist (Gd-DTPA), followed by serial MR imaging over the course of 10-12 hours. The purpose of the study is determine the transport kinetics of Central Nervous System (CNS) exposure to gadolinium contrast injected into the lumbar intrathecal space (lower back) and evaluate changes with age. This will allow investigators to evaluate the brain parenchymal penetration of gadolinium as an illustrative imaging marker that mirrors the glymphatic system. Investigators hypothesize the exposure and penetration patterns of the neuraxis to neurotherapeutic drugs can be modeled using gadolinium intrathecal contrast administered in the lumbar intrathecal space.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Deemed healthy and able to undergo MR imaging by the Site Investigator, based on screening assessments:
- •medical history, physical examination, vital signs, and clinical laboratory values
- •Willing to undergo multiple imaging sessions
- •Normal screening MRI to exclude subjects with a mass (e.g., disk herniation), congenital malformation (e.g., Chiari malformation), or an abnormal curvature of the spine that could alter CSF flow.
- •If female of childbearing age: negative pregnancy test
- •Normal Basic metabolic Panel and CBC (Platelet count \> 150,000; Hb \>8)
- •Willing to undergo LP procedure. -
Exclusion Criteria
- •Claustrophobia
- •Chronic cough
- •Active infection with fever (\>101.5), to limit risk of meningitis. Infections could include pneumonia, pharyngitis, skin infection, UTI, etc.
- •History of CNS tumor or anomaly
- •History of radiation therapy to the CNS
- •History of hydrocephalus
- •Abnormality on MRI that could impede CSF flow (i.e., extruded disk)
- •Laboratory finding of prolonged coagulation times
- •Pregnant/nursing
- •Prior spine or brain surgery or trauma
Outcomes
Primary Outcomes
Drug distribution over time
Time Frame: 6 time-points over 12 hours
The drug distribution of gadolinium contrast throughout the Central Nervous System over time (12 hours)