Impact of Vitamin D Supplementation in Patients With Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Relapsing-Remitting, Vitamin D Deficiency
Status
Completed
Phase
Phase 4
Locations
Slovenia
Study Type
Interventional
Intervention
Vitamin D
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Sclerosis, Relapsing-Remitting
Eligibility Criteria
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
Sites / Locations
- University Medical Centre Maribor
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1000 IU of vitamin D per day
4000 IU of vitamin D per day
Arm Description
Half of randomized patients will receive 1000 IU of vitamin D per day
Half of randomized patients will receive 4000 IU of vitamin D per day
Outcomes
Primary Outcome Measures
Vitamin D supplementation dose response
Change in vitamin D level in serum after supplementation with 1000IU/day or 4000 IU/day.
Secondary Outcome Measures
Full Information
NCT ID
NCT03385356
First Posted
December 20, 2017
Last Updated
March 18, 2019
Sponsor
University Medical Centre Maribor
Collaborators
Medical Faculty Maribor
1. Study Identification
Unique Protocol Identification Number
NCT03385356
Brief Title
Impact of Vitamin D Supplementation in Patients With Multiple Sclerosis
Official Title
Impact of Vitamin D Supplementation in Patients With Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
December 19, 2017 (Actual)
Primary Completion Date
April 30, 2018 (Actual)
Study Completion Date
April 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Centre Maribor
Collaborators
Medical Faculty Maribor
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Relapsing-Remitting, Vitamin D Deficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
1000 IU/day of Vitamin D vs 4000 IU of Vitamin D /day; IU (international units)
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
89 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1000 IU of vitamin D per day
Arm Type
Active Comparator
Arm Description
Half of randomized patients will receive 1000 IU of vitamin D per day
Arm Title
4000 IU of vitamin D per day
Arm Type
Active Comparator
Arm Description
Half of randomized patients will receive 4000 IU of vitamin D per day
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Other Intervention Name(s)
Oleovit D3
Intervention Description
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.
Primary Outcome Measure Information:
Title
Vitamin D supplementation dose response
Description
Change in vitamin D level in serum after supplementation with 1000IU/day or 4000 IU/day.
Time Frame
4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Saša Gselman, MD
Organizational Affiliation
University Medical Centre Maribor
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Centre Maribor
City
Maribor
ZIP/Postal Code
2000
Country
Slovenia
12. IPD Sharing Statement
Learn more about this trial
Impact of Vitamin D Supplementation in Patients With Multiple Sclerosis
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