Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
10 participants
OBSERVATIONAL
2024-07-01
2028-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Interventions
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No interventinon
No intervention is anticipated. This is an observational study.
Eligibility Criteria
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Inclusion Criteria
* Calculated GFR greater or equal to 60 mL/min/1.73 m2
Exclusion Criteria
* 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)
18 Years
89 Years
ALL
No
Sponsors
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Oregon Health and Science University
OTHER
Responsible Party
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Juan Piantino
Associate Professor
Other Identifiers
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IT Gadolinium Study
Identifier Type: -
Identifier Source: org_study_id
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