NCT01512537已完成不适用
Comparison of UVB and Vitamin D Supplementation in Treatment of Vitamin D Deficiency
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 2
- 主要终点
- Vitamin D (nmol/l).
研究概览
简要总结
The purpose of the study is to compare the efficiency of UVB and vitamin D supplementation in treatment of vitamin D deficiency.
详细描述
Patients with vitamin D deficiency were recruited and randomized into two groups, one exposed to UVB and the other receiving oral treatment with vitamin D supplementation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 15 Years 至 70 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Vitamin D deficiency (< 25 nmol/l)
- •Age 15 or above
排除标准
- •Travel south of 45 degrees latitude during the trial.
- •Ongoing treatment with vitamin D supplementation.
- •Intake of light sensitive medicine, such as tetracyclins.
- •Skin light eruptions
结局指标
主要结局
Vitamin D (nmol/l).
时间窗: Week 0
Vitamin D was measured in a bloodsample to determine baseline status.
Vitamin D (nmol/l)
时间窗: Week 3
Vitamin D was measured in a bloodsample to follow the change from baseline in vitamin D level at week 3.
Vitamin D
时间窗: Week 6
Vitamin D was measured in a bloodsample to follow the change from baseline in vitamin D level at week 6.
次要结局
- Parathyroid hormone (pmol/l).(Week 0, 3 and 6.)
- Albumin (g/l).(Week 0, 3 and 6.)
- Calcium (mmol/l)(Week 0, 3 and 6.)
- Hemoglobin A 1c (percentage HbA1c of total hemoglobin).(Week 0, 3 and 6.)
研究者
Morten Bogh
Principal Investigator
Lund University
研究点 (2)
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