Efficacy of Vitamin D Supplementation in relapsing-remitting Multiple Sclerosis

Stopped earlyPhase 2Relapsing MS2011-002785-20

What it found

Stopped

The trial ended early for another reason (see below).

18 months

Read by software from the paper's abstract

What was tested

Treatment tested

  • Cholecalciferol

    Vitamin D receptor agonist

What it measured

Main measures

  • Cumulative number of new hyperintense lesions in T2-weighted cranial MR imaging

    MRI lesions

Other measures (1)

  • Annualized relapse rate, proportion of relapse-free patients, disease progression, percentage of patients without disease activity, proportion of patients with a conversion into a definitive MS (only in CIS patients), other MRI parameters (number / volume of new hypointense T1 lesions, brain atrophy, number of lesions absorbing contrast agent, spectroscopy) cognition, fatigue, depression, Retinal

    RelapsesMRI lesionsBrain volume lossRetina scans (OCT)Thinking and memoryFatigueMood and sleepQuality of life (reported by participants)

Who could take part

Relapsing MS

Show the full criteria

Inclusion criteria

Inclusion: Informed consent Exclusion: Any other MS-course than RRMS

Exclusion criteria

Not separately supplied in the registry.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

To assess efficacy of Vitamin D supplementation in relapsing-remitting Multiple Sclerosis

Papers

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History

    1. Started

      Aug 2011

    Assembled by software from public sources.