View Clinical Trial (Medical Research Study)
Oral Megadose Corticosteroid Therapy of Acute Exacerbations of Multiple Sclerosis (OMEGA)
| City: |
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New York |
| State: |
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New York |
| Zip Code: |
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10029 |
| Conditions: |
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Multiple Sclerosis |
| Purpose: |
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This clinical trial compares the relative efficacy of treating acute exacerbations of
relapsing forms of Multiple Sclerosis with equivalent doses of oral and intravenous (IV)
methylprednisolone. This is a randomized, blinded, multi-center study.
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| Study Summary: |
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Intravenous methylprednisolone has been the standard of care for treating acute MS flares.
However, the IV administration is cumbersome, inconvenient and expensive. A true comparison
of these different approaches has not been undertaken in rigorous fashion. Prior studies
have demonstrated the safety of such high doses of oral steroid. For this proposal we employ
equivalent oral dosing (1400 mg/day) and compare that to 1000 mg/day IV therapy in patients
seen within seven days of an acute exacerbation of MS.
In addition, there are 2 arms to this double-blind, placebo controlled, randomized trial.
One arm has an active IV and an oral placebo while the second arm has an IV placebo and an
active oral dose. Therefore, each subject will receive an active treatment.
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| Criteria: |
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Inclusion Criteria:
- Between the ages of 18 and 50 years, inclusive.
- Acute symptomatic exacerbation of MS present for great than 24 hours and less than or
equal to 7 days at entry with new or worsening symptoms, and with signs referable to
the symptoms; in the absence of a fever or active infection.
- Diagnosis of a relapsing form of multiple sclerosis before randomization as
determined by Poser or McDonald Criteria.
- Expanded disability status scale (EDSS) score between 2 and 6.5, inclusive at entry.
- Episodes include study neurologist or neuro-ophthalmologist diagnosed: acute optic
neuritis, cerebellar, brainstem dysfunction, myelitis, focal cerebral, and/or
definitive focal sensory dysfunction.
- New objective clinical finding other than a sensory exacerbation, or bowel/bladder
signs alone. Sensory deficits alone will not qualify except for optic neuritis.
- Subjects may continue on their current immunomodulating therapy (such as interferons
or glatiramer acetate) throughout the course of the study. Women who become pregnant
after the 5-day treatment of steroids should discontinue immunomodulatory treatment.
- Understand and sign written informed consent prior to any testing under this
protocol, including screening tests and evaluations that are not considered part of
the subject's routine care.
Exclusion Criteria:
- Any patients treated with systemic corticosteroid use within one month of the index
episode at screening.
- Prior use of immunosuppressive treatments within 90 days of index episode
(mitoxantrone, azathioprine, IVIg) or plasmapheresis.
- Any patient who is pregnant or breastfeeding.
- Unable to perform the Multiple Sclerosis Functional Composite consisting of: Timed
25-Foot Walk, 9-Hole Peg Test, and Paced Auditory Serial Addition Test (3 second).
- Peripheral or cranial neuropathy as sole problem of acute episode.
- History of any significant cardiac, gastrointestinal, hepatic, pulmonary, or renal
disease; immune deficiency; or other medical conditions that would preclude
corticosteroid therapy.
- Primary Progressive Multiple Sclerosis (PPMS).
- Previous participation in this study.
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| NCT ID: |
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NCT00418145 |
| Primary Contact: |
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Principal Investigator
Fred Lublin, MD
Mount Sinai School of Medicine
Tarah Gustafson
Phone: 212-241-4264
Email: tarah.gustafson@mssm.edu
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| Backup Contact: |
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N/A |
| Location Contact: |
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New York, New York 10029
United States
Tarah Gustafson
Phone: 212-241-4264
Email: tarah.gustafson@mssm.edu
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 21, 2013 |
| Modifications to this listing: |
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