Isfahan University of Medical Sciences

CompletedNot a drug-phase studyRelapsing MSNCT02696590

What it found

No results found

We found no results in the registry or in papers.

This trial finished 11 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

  • Cholecalciferol

    Vitamin D receptor agonist

What it measured

Main measures

  • Serum concentration of 25(OH)D

    Two Weeks

    How the body handles the medicine

Who could take part

Relapsing MS · 23 to 59

Show the full criteria

Inclusion criteria

* with serum 25(OH)D3 concentration ≤ 20 ng/ml

Exclusion criteria

* hypercalcaemia, primary hyperparathyroidism, Paget disease, thyrotoxicosis, pregnancy, active malignancy, hypercalciuria, history of liver disease, renal insufficiency, clinically apparent malabsorption syndrome, using drugs containing vitamin D products, calcium, estrogen and drugs known to affect vitamin D metabolism (anticonvulsants, glucocorticoids) or receiving any form of supplements containing vitamin D during last 6 months. * Participants with serum 25(OH)D concentration≥ 20 ng/ml

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

About this trial

In the sponsor's words

This study aimed to evaluate oral and injectable routes in treatment of hypovitaminosis D in multiple sclerosis (MS) patients. The investigators aimed to assess the efficacy of each method, using the same Mega dose of 600 000 IU D3, in achieving normal serum 25(OH)D level, the durability of the response, the practicality and the possible toxicity.

Papers

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    Related trials

    History

      1. Started

        Jul 2015

      2. Main results due

        Nov 2015

      3. Finished

        Dec 2015

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