Efficacy of the Dose Regimen of Oral Vitamin D 50,000 IU in the Treatment of Vitamin D Deficiency
Status:
Unknown status
Trial end date:
2014-11-01
Target enrollment:
Participant gender:
Summary
Abstract:
The main objective of the proposed study is to examine the Safety and Efficacy Evaluation of
the Dose Regimen of Vitamin D 50,000 IU (Biodal) tablet supplementation in the treatment of
population with vitamin D deficiency.
A randomized, double-blind placebo, Parallel design comparing vitamin D with Placebo will be
conducted on 60 Healthy males and females with vitamin D deficiency, age from 18 to 49 years
who attend the rehabilitation clinics at Jordan University Hospital .Participants who met the
inclusion criteria will be asked to sign an informed witnessed consent form. Results obtained
are expected to assess the safety and efficacy of the dose regimen used in this study as per
Biodal SmPC. This study will also contribute to the global body of knowledge in this field.
The major findings generated from this study could open certain avenues for further research
through the association of the status of vitamin D in serum .
Phase:
Phase 2
Details
Lead Sponsor:
Hayat Pharmaceutical Co. PLC
Treatments:
Cholecalciferol Ergocalciferols Vitamin D Vitamins