Role of Vitamin D in Reducing the Relapse Rate in Patients With Multiple Sclerosis
Primary Purpose
Multiple Sclerosis
Status
Unknown status
Phase
Phase 2
Locations
Saudi Arabia
Study Type
Interventional
Intervention
Vitamin D3
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, Relapsing rate, Expanded disability status scale, Vitamin D3
Eligibility Criteria
Inclusion Criteria:
- Age between 18-55 years
- Confirmed Multiple Sclerosis diagnosis according to McDonald criteria
- Stable neurological functioning for at least one month prior to study entry
- Expanded Disability Scale score (EDSS) less than <_4.0
- Must have had one clinical attack in past two years and at least one new silent T2 or gadolinium-enhancing lesion on MRI within the past one year.
- Willing to participate for the entire 52-week period
Exclusion Criteria:
- pregnant or nursing.
- Connective tissue disease (SLE, Sjogren's disease)
- Endocrine disease (hyperthyroidism, hyperparathyroidism)
- Any medical condition predisposing to hypercalcaemia, nephrolithiasis or renal insufficiency
Sites / Locations
- Multiple Sclerosis clinic, Department of Neurology, King Khalid Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Vitamin D3
Placebo
Arm Description
Administered orally on weekly basis
To be administered orally on weekly basis
Outcomes
Primary Outcome Measures
Relapse rate in patients with Multiple Sclerosis
Secondary Outcome Measures
Improvement in the expanded disability status scores after receiving vitamin D3
Full Information
NCT ID
NCT01753375
First Posted
December 17, 2012
Last Updated
December 17, 2012
Sponsor
AlJohara M AlQuaiz, M.D.
1. Study Identification
Unique Protocol Identification Number
NCT01753375
Brief Title
Role of Vitamin D in Reducing the Relapse Rate in Patients With Multiple Sclerosis
Official Title
Role of Vitamin D on the Relapse Rate of Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Unknown status
Study Start Date
January 2013 (undefined)
Primary Completion Date
July 2014 (Anticipated)
Study Completion Date
October 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
AlJohara M AlQuaiz, M.D.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Vitamin D3 supplementation reduces the incidence of multiple sclerosis.Although clinical cross-sectional studies have demonstrated vitamin D3 as a positive mediator in preventing relapses and disease progression, prospective randomized control trials are nevertheless necessary to confirm these statements and to determine the most efficacious, safe, and the minimum required doses. This hypothesis is going to be tested through a randomized triple blinded controlled trial in which after randomization, one group of patients will receive vitamin D and second group will receive placebo. Both groups are going to be followed in a similar way over a period of one year with follow ups at 4, 8 and 12 months. Vitamin D levels is going to be performed at 0,4, 12 month interval. MRI is going to be done at the beginning and end of trial.The number of relapses and the physical disability will be calculated through the Expanded disability status scale (EDSS).
Detailed Description
Study Objectives:
To estimate the prevalence of vitamin D deficiency in Saudi Multiple Sclerosis(MS) patient coming to King Khalid hospital, multiple sclerosis clinic.
To compare the difference in the relapse rate among Multiple Sclerosis patients who are taking vitamin D3 (50,000 IU per week) versus those who are not taking Vitamin D3 supplements.
To assess and compare the improvement in the Expanded Disability Status scale and clinical symptoms among those who are taking vitamin D3 versus those who are on placebo
Study Design: A single centre, triple-blinded, parallel randomized placebo controlled trial.
Methods: All eligible patients with clinical definite MS will be assigned a computer-generated Identification number by the statistician and through randomization divided into two groups, one group receiving vitamin D3 (the intervention arm) and other getting placebo (the control arm). All patients will continue with their routine pre-intervention trial treatment for relapse and remission phases of multiple sclerosis. The first treatment group will receive 50,000 IU units of vitamin D3 per week . The control arm patients, instead of vitamin D3 will receive a placebo supplement that looks, smells and tastes the same as the vitamin D3 for 52 weeks. Compliance with the study treatment will be verified by asking the patients about missed doses and by counting used and unused bottles.
All patients will be asked questions related socio-demographic data, vitamin D related dietary products, physical activity questions, exposure to sunlight and variation according to season, use of sunscreen, body coverage when in sunlight and any previous treatment for Multiple Sclerosis, including any vitamin D supplements. Every follow up visit shall include documentation of complete neurologic and medical history and findings. This will be a triple-blinded trial. The patient, the treating physician and the statistician will be masked to the type of treatment each patient receives.Sealed envelopes containing the vitamin D3 or placebo are going to be handed over to the physician with the computer assigned number of the patient. At each follow-up visit all patients will be required to bring their envelopes along with empty/ filled bottles to assess their compliance with the treatment.
The treating physician will follow all the patients at set regular intervals: 0 (baseline), 4, 8, and 12 months to assess the relapses and the EDSS scores and also to check for any adverse effects arising because of the vitamin D3 supplements. Patients who are going to miss their appointment shall be contacted by the project staff to set another appointment in the subsequent week. All patients are going to be emphasized about the importance of these clinical visits and their compliance with the treatment. All patients will be evaluated by the same treating physician.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple Sclerosis, Relapsing rate, Expanded disability status scale, Vitamin D3
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Vitamin D3
Arm Type
Active Comparator
Arm Description
Administered orally on weekly basis
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
To be administered orally on weekly basis
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Intervention Description
Vitamin D3 given as 50000 IU orally on weekly basis
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo to be given orally on weekly basis
Primary Outcome Measure Information:
Title
Relapse rate in patients with Multiple Sclerosis
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Improvement in the expanded disability status scores after receiving vitamin D3
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age between 18-55 years
Confirmed Multiple Sclerosis diagnosis according to McDonald criteria
Stable neurological functioning for at least one month prior to study entry
Expanded Disability Scale score (EDSS) less than <_4.0
Must have had one clinical attack in past two years and at least one new silent T2 or gadolinium-enhancing lesion on MRI within the past one year.
Willing to participate for the entire 52-week period
Exclusion Criteria:
pregnant or nursing.
Connective tissue disease (SLE, Sjogren's disease)
Endocrine disease (hyperthyroidism, hyperparathyroidism)
Any medical condition predisposing to hypercalcaemia, nephrolithiasis or renal insufficiency
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Prof. Abdulkader Daif, M.D
Phone
0966-0504205164
Email
adaif@ksu.edu.sa
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
AlJohara M AlQuaiz, M.D
Organizational Affiliation
King Saud University- Medical college
Official's Role
Principal Investigator
Facility Information:
Facility Name
Multiple Sclerosis clinic, Department of Neurology, King Khalid Hospital
City
Riyadh 11321
ZIP/Postal Code
231831
Country
Saudi Arabia
12. IPD Sharing Statement
Citations:
PubMed Identifier
8755567
Citation
Cantorna MT, Hayes CE, DeLuca HF. 1,25-Dihydroxyvitamin D3 reversibly blocks the progression of relapsing encephalomyelitis, a model of multiple sclerosis. Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7861-4. doi: 10.1073/pnas.93.15.7861.
Results Reference
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PubMed Identifier
11115787
Citation
Hayes CE. Vitamin D: a natural inhibitor of multiple sclerosis. Proc Nutr Soc. 2000 Nov;59(4):531-5. doi: 10.1017/s0029665100000768.
Results Reference
background
PubMed Identifier
14718698
Citation
Munger KL, Zhang SM, O'Reilly E, Hernan MA, Olek MJ, Willett WC, Ascherio A. Vitamin D intake and incidence of multiple sclerosis. Neurology. 2004 Jan 13;62(1):60-5. doi: 10.1212/01.wnl.0000101723.79681.38.
Results Reference
background
PubMed Identifier
17823429
Citation
Kimball SM, Ursell MR, O'Connor P, Vieth R. Safety of vitamin D3 in adults with multiple sclerosis. Am J Clin Nutr. 2007 Sep;86(3):645-51. doi: 10.1093/ajcn/86.3.645.
Results Reference
background
PubMed Identifier
22567287
Citation
Shaygannejad V, Janghorbani M, Ashtari F, Dehghan H. Effects of adjunct low-dose vitamin d on relapsing-remitting multiple sclerosis progression: preliminary findings of a randomized placebo-controlled trial. Mult Scler Int. 2012;2012:452541. doi: 10.1155/2012/452541. Epub 2012 Apr 11.
Results Reference
background
PubMed Identifier
21154396
Citation
Jagannath VA, Fedorowicz Z, Asokan GV, Robak EW, Whamond L. Vitamin D for the management of multiple sclerosis. Cochrane Database Syst Rev. 2010 Dec 8;(12):CD008422. doi: 10.1002/14651858.CD008422.pub2.
Results Reference
background
PubMed Identifier
20427749
Citation
Burton JM, Kimball S, Vieth R, Bar-Or A, Dosch HM, Cheung R, Gagne D, D'Souza C, Ursell M, O'Connor P. A phase I/II dose-escalation trial of vitamin D3 and calcium in multiple sclerosis. Neurology. 2010 Jun 8;74(23):1852-9. doi: 10.1212/WNL.0b013e3181e1cec2. Epub 2010 Apr 28. Erratum In: Neurology. 2010 Aug 3;75(5):480. Neurology. 2010 Sep 14;75(11):1029. Dosage error in article text.
Results Reference
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Role of Vitamin D in Reducing the Relapse Rate in Patients With Multiple Sclerosis
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