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临床试验/CTRI/2017/10/010187
CTRI/2017/10/010187已完成不适用

To evaluate the efficacy of micellized vitamin D3 versus fat soluble vitamin D3 in vitamin D deficient adults and elderly with type IV& V skin.

International Life Sciences Institute India1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2016年10月30日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
1
主要终点
To evaluate the efficacy of micellized vitamin D3 versus

研究概览

简要总结

In this randomized prospective study, we aim to evaluate the efficacy of micellized vitamin D over non-micellized Vitamin D in adults and elderly. Two hundred healthy adults (100 males and 100 females) and 200 healthy (100 males and 100 females) elderly individuals females), with vitamin D deficiency ( serum 25 (OH) D < 20 ng/mL) will be included in this study. A thorough history will be taken followed by a detailed clinical and systemic examination. Vitamin D3 supplementation will be given 60000 IU every month in a randomized manner with either micellized or non-micellized of vitamin D3 for a period of 12 months . Blood samples will be collected at baseline and after 6 & 12 months of supplementation. The samples will be analyzed for serum 25(OH) D, parathyroid hormone (PTH), calcium, phosphates, alkaline phosphatase, bone markers (serum PINP & CTX) and inflammatory markers (IL-1, 2, 6 and 10, IFN- γ, ultrasensitive CRP & TNF-α). Urine samples collected at baseline and after 6 & 12 months of supplementation with oral cholecalciferol, were analyzed for calcium creatinine ratio.

Results:

Eighty-nine subjects in group A and 77 in group B completed the trial. Subjects in both  groups had  significant increase in their serum 25(OH)D levels following supplementation (Group A: 8.6 ± 4.4 ng/mL to 30.7 ± 7.5 ng/mL (p < 0.001); Group B: 9.1 ± 4.1 to 23.1 ± 6.4 ng/mL (p < 0.001). Participants in micellized group had an additional increase of 8.1 ng/mL in serum 25(OH)D levels (p<0.001). Eighty one  (91%) subjects in group A and fifty two (67%) in group B achieved serum 25(OH)D >20ng/ml (p <0.0001) following supplementation. No hypercalcemia or hypercalciurea was noted during the trial.

Conclusion:

Supplementation with both micellized and non-micellized vitamin D3 result in a significant rise in serum 25(OH)D levels. Micellized vitamin D3 appears to be more efficacious.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Adults and elderly with vitamin D deficiency.

排除标准

  • Subjects suffering from any systemic disorders affecting the bone mineral health.
  • Adults and elderly consuming calcium, vitamin D or other medications like ATT, anticonvulsants etc, which are likely to impact bone mineral metabolism.

结局指标

主要结局

To evaluate the efficacy of micellized vitamin D3 versus

时间窗: After 6 and 12 months of supplementation

fat soluble vitamin D3 in adults and elderly with known

时间窗: After 6 and 12 months of supplementation

vitamin D deficiency

时间窗: After 6 and 12 months of supplementation

次要结局

  • Effect of vitamin D3 supplementation on bone markers((PINP, NTX) and inflammatory markers (ultrasensitive)

研究者

发起方
International Life Sciences Institute India
申办方类型
Other [Non-profitable Non-governmental Organization]

研究点 (1)

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