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.
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)
