Study to Compare the Clinical and Radiological Efficacy of 625 mg Versus 1250 mg of Oral Methylprednisolone in Patients With Multiple Sclerosis in Relapse

DESIGN: Phase IV clinical trial, multicentre, randomized and double blind, active drug controlled and parallel groups. Patients will be randomised to a high dose of oMP vs a lower-high dose of oral Methylprednisolone (oMP).

SETTING: 9 MS Units from 9 hospitals of the public health system with extensive experience in treating patients with MS and design and participation in clinical trials.

PROCEDURES:

After signing the informed consent, the inclusion and exclusion criteria specific to the study will be checked. The diagnostic test will take place prior to administration of study medication and will include medical history, neurological examination (EDSS measurement) taking of vital signs (blood pressure, heart rate and body temperature) and MRI. Concomitant medication will be checked. Patients will be instructed about the requirements during the study.

The trial medication will be provided to the patient in the medical office (day 1 of the study), where the patient will remain until the intake. This action will be repeated the following 2 days. The latency period from the beginning of the relapse until the start of treatment will be registered. The questionnaires of tolerance will be completed.

Day 1 will be defined as the first day on which first dose of oMP is administered.

Once given the treatment under study, the adverse events reported spontaneously or after question will be collected.

There will be follow-up visits at 7 and 28 days, and 3 months after initiation of treatment. At baseline, prior to drug administration, and on days 7 and 28 after initiation of treatment, a brain MRI with and without contrast will be performed. In case of adverse events or laboratory abnormalities, the patients could have an accessory follow-up visits until resolution.

Randomization will be performed on the day of administration (day 1)

The treatments are:

Group A: Methylprednisolone 1250 mg / day orally for 3 days Group B: Methylprednisolone 625 mg / day orally for 3 days

Inclusion criteria

• Relapsing-remitting MS (Mc Donald criteria 2010) regardless being under immunomodulatory treatment
• EDSS (previous to relapse) between 0 and 5
• MS relapse of moderate intensity (EDSS increase from 1 to 2.5 points) or severe intensity (EDSS increase > 3 points)

• If EDSS previous relapse is available:

• optic neuritis, myelitis or brainstem relapse: the EDSS should increase of 1 point in visual, pyramidal or brainstem system function
• relapse in other location or uncertain location: the EDSS should increase at least 1 point
• If EDSS previous relapse is not available:

• optic neuritis, myelitis or brainstem relapse: the visual, pyramidal or brainstem system function should be > 2 points.
• relapse in other location or uncertain location: EDSS should be > 2 points
• Recent clinical relapse onset (<15 days) without fever
• One month of clinical stability prior to relapse
• Signed informed consent
• Capacity to ingest the medication.

Exclusion criteria

• Doubts about the diagnosis of multiple sclerosis
• First episode of inflammatory neurological disease
• Secondary progressive MS or primary progressive MS
• Symptoms with lasted less than 24 hours of evolution
• Any degree of subjective or objective remission
• Treatment with corticosteroids during the previous 30 days
• Patients with immunosuppressive treatment (azathioprine, mitoxantrone, cyclophosphamide) or Natalizumab or Fingolimod
• Pregnancy or breastfeeding women or women of childbearing potential not using contraceptive measures
• Diseases with a contraindication of treatment with corticosteroids
• History of serious adverse reaction or hypersensitivity to drugs related to study medication
• Patients who could not be regular MRI, not collaborators or who requires anesthesia.
• Lactose intolerance
• Patients with allergies to contrast used in MRI
• Patients with renal impairment