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Clinical Trial Summary

Patients will undergo magnetic resonance spectroscopy (MRS) scanning to noninvasively measure intracerebral and plasma metabolite levels at baseline and following 2 and 4 hours of hyperglycemia. Subjects will also undergo a lumbar puncture at a separate occasion to assess cerebrospinal fluid levels of metabolites.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02272556
Study type Interventional
Source Yale University
Contact
Status Completed
Phase N/A
Start date February 2015
Completion date May 18, 2022

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