Multiple Sclerosis Clinical Trial

Quantitative Imaging and Proton Spectroscopy in Multiple Sclerosis

Summary

The primary purpose of this study is to detect changes in the brain that may be associated with multiple sclerosis. Results will be compared to age matched controls. Investigators will assess lesions by measuring T2 and T1 enhanced lesion volumes and magnetization transfer ratio histogram parameters (MTRHP) in patients with relapsing-remitting and secondary-progressive disease. This data will be correlated to total brain parenchymal volume as well as identifying the effect of MS lesions on the gray and white matter, volumetric disability, including Kurtzke Expanded Disability Status Scale (EDSS) and a specific battery of neuropsychological tests. Quantitative analysis of whole brain N-acetylaspartate (WBNAA), a reproducible measure of viable neuron number, using 1H MRS and compare the results to age-matched controls over duration of 5 years.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with known MS diagnosis
Age 7-110 years
Males or females

Exclusion Criteria:

Medically unstable
Artificial implants in the body
Pregnant

Normal Controls

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

69

Study ID:

NCT01226654

Recruitment Status:

Terminated

Sponsor:

NYU Langone Health

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There is 1 Location for this study

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NYU Langone Medical Center
New York New York, 10016, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

69

Study ID:

NCT01226654

Recruitment Status:

Terminated

Sponsor:


NYU Langone Health

How clear is this clinincal trial information?

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