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OpenTrials
Completed

NCT Number: NCT03385356

Impact of Vitamin D Supplementation in Patients With Multiple Sclerosis

Vitamin D is important risk factor for developing multiple sclerosis (MS) and for disease progression. Patients with MS who had lower vitamin D levels were at increased risk for more clinical attacks and faster disease progression. It was also shown that patients with MS had lower vitamin D levels in serum than healthy controls. It is not clearly defined, which are the levels of vitamin D in serum, that are high enough to trigger immunomodulatory effect and are safe for patients.

This double-blind randomized clinical trial was designed to compare impact of vitamin D supplementation in two different doses (1000 IU/day vs 4000 IU/day) in patients with relapsing remitting MS. The main goal of this trial is to compare dose response on vitamin D supplementation and to estimate more closely appropriate level of vitamin D in serum which triggers some of experimentally shown immunomodulatory actions.

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Key information

About this study

Vitamin D is important risk factor for developing multiple sclerosis (MS) and for disease progression. Patients with MS who had lower vitamin D levels were at increased risk for more clinical attacks and faster disease progression. It was also shown that patients with MS had lower vitamin D levels in serum than healthy controls. It is not clearly defined, which are the levels of vitamin D in serum, that are high enough to trigger immunomodulatory effect and are safe for patients.

This double-blind randomized clinical trial was designed to compare impact of vitamin D supplementation during four months in winter time in two different doses (1000 IU/day vs 4000 IU/day) in patients with relapsing remitting MS. The main goal of this trial is to compare dose response on vitamin D supplementation and estimate more closely appropriate level of vitamin D in serum which triggers some of experimentally shown immunomodulatory actions. To define immunomodulatory response different laboratory, clinical and genetic tests will be performed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Relapsing remitting MS
  • Treatment with immunomodulatory drug
  • Age 18-60 years and
  • EDSS (Expanded Disability Status Scale) score less than 5.

Exclusion criteria

  • Use of vitamin D supplements in the past 3 months
  • Pregnancy, planning pregnancy or nursing
  • Relapse of disease and corticosteroids use in past month
  • Active inflammation at the start of the study (flu, cystitis etc.)
  • Renal disease
  • Elevated levels of calcium or parathormone
  • Hypersensitivity to vitamin D preparations
  • Switching of immunomodulatory drug in past 3 months
  • Other autoimmune disease
  • History of hyperparathyroidism, liver disease, tuberculosis, sarcoidosis or kidney stones

Treatment and study plan

Vitamin D

Drug

Vitamin D supplementation of 1000IU vs 4000IU vitamin D per day for four months during winter time, when levels of vitamin D in serum of MS patients are especially low.

Other names: Oleovit D3

Primary outcomes

  1. Vitamin D supplementation dose response

    Time frame: 4 months

    Change in vitamin D level in serum after supplementation with 1000IU/day or 4000 IU/day.

Sponsors and collaborators

Lead sponsor

University Medical Centre Maribor

Other

Collaborators

  • Medical Faculty Maribor

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Dec 28, 2017
Registry last updated
Mar 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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