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临床试验/NCT02091219
NCT02091219已完成早期 1 期

The Effects of Vitamin D3 Versus 25OHD3 (HyD) on Serum Vitamin D Metabolites and Markers of Mineral Metabolism and Immune Function

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2014年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
35
试验地点
2
主要终点
Change in total serum 25D

研究概览

简要总结

The purpose of this study is to compare the effects of two different forms of vitamin D supplements (vitamin D3 and 25-hyrdroxyvitamin D3 [25(OH)D3]) on vitamin D levels in the blood, and on markers of skeletal and immune health. This study is designed as a pilot study. A multi-ethnic cohort of 48 patients will be included (12 Caucasian, 12 African American, 12 Hispanic/Latino, 12 Asian/Asian American). Potential study candidates will undergo a screening visit during which a medical history will be taken, a physical exam performed, a dietary questionnaire administered, and blood collected. The purpose of the screening visit is to identify vitamin D-deficient (25-hydroxyvitamin D <20 ng/ml) individuals who are candidates for vitamin D supplementation. Eligible patients will then be randomly assigned to receive either vitamin D3 (2400 IU/day) or 25(OH)D3 (20 mcg/day) for 16 weeks. After initiating supplementation, study patients will return for follow-up visits at weeks 4, 8, and 16. At each visit, blood will be collected to assess vitamin D levels in the blood, as well as markers of skeletal and immune function. Participation in this study will therefore involve a total of 5 visits (1 screening visit, 1 randomization visit during which participants will receive their study supplements, 3 follow-up visits). After all data is collected, changes in vitamin D levels in the blood following supplementation with either vitamin D3 versus 25(OH)D3 will be determined, and correlated to markers of calcium balance and immune function. Knowledge gained from this study may have a significant impact on how vitamin D status is defined, and how vitamin D repletion is administered.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18
  • 25D < 20 mg/ml

排除标准

  • Age < 18
  • 25D > 20 ng/ml at time of screening
  • Clear signs of infection at time of screening (coughing, sneezing, wheezing, frequency, dysuria)
  • History of conditions that would influence intestinal absorption of vitamin D3 or 25OHD3 supplements
  • History of nephrolithiasis, primary hyperparathyroidism, or other metabolic bone disease
  • History of chronic kidney disease (defined as CrCl < 30 ml/min)
  • History of rheumatologic or autoimmune conditions
  • History of sarcoidosis
  • History of active or latent tuberculosis
  • History of HIV
  • History of hyperthyroidism
  • History of chronic glucocorticoid use defined as the equivalent of 5 mg of prednisone per day for more than 2 months within the last 6 months
  • History of use of medications known to affect calcium/vitamin D metabolism, bone metabolism, and immune response
  • Hypercalcemia
  • Hypercalcinuria

研究组 & 干预措施

25(OH)D3

Experimental

20 micrograms/day by mouth for 16 weeks

干预措施: 25(OH)D3 (Drug)

Vitamin D3

Experimental

2,400 IU/day by mouth for 16 weeks

干预措施: Vitamin D (Drug)

结局指标

主要结局

Change in total serum 25D

时间窗: 16 weeks

次要结局

  • Change in total free 1,25D(16 weeks)
  • Change in urinary calcium(16 weeks)
  • Change in serum free 25D(16 weeks)
  • Change in serum total 1,25D(16 weeks)
  • Change in serum calcium(16 weeks)
  • Change in serum bone turnover markers(16 weeks)
  • Change in markers of immune function(16 weeks)
  • Change in serum iPTH(16 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Adams, M.D.

Professor, Department of Orthopaedic Surgery

University of California, Los Angeles

研究点 (2)

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