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Comparing the effect of high dose vitamin D3 intake on interleukin-10, 17 and quality of life in Multiple Sclerosis patients

Comparing the effect of high dose vitamin D3 intake on interleukin-10, 17 and quality of life in Multiple Sclerosis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015010910891N2
Enrollment
45
Registered
2015-08-19
Start date
2013-12-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis.

Interventions

Intervention 1: Intervention group 1: 50,000IU vitamin D every five days, for 3 months vitamin D pearl Zahravi Pharmaceuticals. Intervention 2: Control group: placebo tablet, including inert su
Treatment - Drugs
Placebo
Intervention group 1: 50,000IU vitamin D every five days, for 3 months vitamin D pearl Zahravi Pharmaceuticals
Control group: placebo tablet, including inert substance one every five days, made by a Pharmacist

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: a definite diagnosis of Relapsing-remitting Multiple Sclerosis (RRMS) according to Mc Donald criteria? age 18 to 55 years? EDSS (Expanded Disability Status Scale) score of less than 4? no relapse 30 days before inclusion? negative ß-HCG test for women in child bearing age. Exclusion criteria: pregnancy? lactation? any other disease than Multiple Sclerosis? receiving>4000IU/d vitamin D? past history of renal or hepatic disease? relapse during the study? received corticosteroids in the previous 30 days? Calcium (Ca)>11mg/dl? Aspartate Transaminase(AST) or Alanine Transaminase(ALT)>3 times normal values? alkaline phosphatase (ALP)>2.5 times normal values.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Interleukin 10, 17. Timepoint: At baseline and after 3 months. Method of measurement: Blood sample.

Secondary

MeasureTime frame
Quality of life. Timepoint: 3 months. Method of measurement: MSQOL54.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFereshteh Ashtari

Isfahan University of Medical Sciences

f_ashtari@med.mui.ac.ir+98 31 3235 0001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026