Not yet recruiting NCT06452459

Glymphatic MRI Study

— Observational Sleep Deprivation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: No interventinon.
Who it may be relevant to: Registry conditions: Sleep Deprivation. Basic parameters: 18 years — 89 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Center list to be confirmed — check the primary protocol.
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Official title

Evaluation of Glymphatic Function With MRI

This study aims at identifying neuroimaging markers of glymphatic function in humans.

Other No interventinon
No intervention is anticipated. This is an observational study.

Inability to obtain consent
Subject is incarcerated, pregnant, or lactating or suspects they may be pregnant
Known allergic or hypersensitivity reactions to gadolinium
Three or more drug allergies from separate drug classes
Recent or expected beed for imaging with iodinated contrast
Contraindications to MRI: claustrophobia, weight greater than maximum MRI scanner capacity, presence of metallic foreign body, or implanted devices not documented as MRI safe
History of neurosurgical procedure or cervical surgery
Current use of anticoagulation medications
Contraindication to lumbar puncture (creatinine or INR elevated above laboratory standard cutoffs)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Center list to be confirmed — check the primary protocol.

NCT: NCT06452459 · IT Gadolinium Study