Pharmacokinetics of Vitamin D in Multiple Sclerosis and in Health
2019年3月1日 更新者:Johns Hopkins University
Pharmacodynamic and Immunologic Effects of Vitamin D Supplementation in Patients With Multiple Sclerosis and Healthy Controls
This is a pilot study of oral vitamin D supplementation to determine if patients with Multiple Sclerosis (MS) and healthy individuals attain a similar increase in serum 25-hydroxyvitamin D levels.
The investigators will also assess whether the immunologic or relevant gene expression response to oral vitamin D supplementation differs in patients with MS and healthy controls.
研究概览
研究类型
介入性
注册 (实际的)
57
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
California
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San Francisco、California、美国、94143
- University of California, San Francisco
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Maryland
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Baltimore、Maryland、美国、21287
- Johns Hopkins University
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-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 60年 (成人)
接受健康志愿者
是的
有资格学习的性别
女性
描述
Inclusion Criteria:
- Female
- Healthy or multiple sclerosis
- Aged 18 to 60
- Body mass index is between 18 kg/m2 and 30 kg/m2
- Screening 25-hydroxyvitamin D level ≤ 75 nmol/L (30 ng/mL)
- White race
- Non-Hispanic ethnicity
- Willing to use birth control during study
- Willing to not use tanning bed during study
If subject has multiple sclerosis:
- Relapsing-remitting MS, as defined by McDonald 2005 criteria
- Screening Expanded Disability Status Scale score ≤ 3.0
- Using no medication for MS, or taking Copaxone, (glatiramer acetate), interferons, or natalizumab
Exclusion Criteria:
- Pregnant or nursing
- Taking multivitamin & unwilling to remain off it during study
- Taking cod liver oil & unwilling to remain off it during study
- On a fat-restricted diet
- History of renal disease or nephrolithiasis (kidney stones)
- History of liver disease
- Taking thiazide diuretics
- History of hyperthyroidism
- History of infection with Mycobacterium species
- History of sarcoidosis
- History of cancer
- History of cardiac disease
- History of HIV
- History of gastrointestinal disorder
- Taking medications that interfere with gastrointestinal absorption
- Cigarette smoker in past month
- Use of illicit drugs in past month
- Use of steroids in past month
- History of hypercalcemia, and screening serum calcium ≤ 10 mg/dL (UCSF) or ≤ 10.7 mg/dL (Johns Hopkins)
- History of hypercalciuria
- Evidence of anemia (Hgb <11.0 g/dL)
- History of other serious medical conditions
- Taking medications that involve the P450 system or may interact with vitamin D (digoxin, diltiazem, verapamil, cimetidine, heparin, or low-molecular weight heparin)
- Other concerns about safety from the perspective of the treating physician
If subject has MS:
-History of major heat sensitivity (leading to sun-avoidant behaviors)
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Vitamin D3
Both those with MS and healthy controls will be given vitamin D3 5000 IU/day by mouth for 90 days.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in Mean Serum Level of 25-hydroxyvitamin D
大体时间:Baseline to 90 days
|
Generalized estimating equations (GEE) with an autoregressive with lag one correlation matrix were used to compare the serially-measured serum 25(OH)D levels between MS patients and Healthy Controls (HCs) to take into account repeated measures and within-subject correlations.
|
Baseline to 90 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in Percentages of T Cell Subsets (IFNγ+ and IL-17+)
大体时间:Baseline, 90 days
|
Analyzed the mean percentage change in IFNγ+ and IL-17+ cluster of differentiation 4 (CD4) + cells (post- versus pre- supplementation).
This represents a change between two time points (90 days versus baseline).
|
Baseline, 90 days
|
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Gene Expression Microarray
大体时间:90 days
|
We had initially planned to do whole blood gene expression.
The experience gained by the laboratory that was to perform this since the original trial was planned was that this measure is too noisy and would not yield meaningful results.
Thus, this analysis will no longer be conducted.
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90 days
|
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Change in Cytokine Levels
大体时间:90 days
|
The original plan had been to measure the change in basic serum cytokine levels (e.g.
IL-17, interferon gamma; IL-10; pg/microliter).
However, due to emerging data suggesting low utility of these measures, this plan was abandoned.
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90 days
|
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Change in Percentage of B Cells
大体时间:90 days
|
The change in percentage (day 90-baseline) was originally planned for study.
Due to the limited number of patients with samples this plan was abandoned.
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90 days
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2010年11月1日
初级完成 (实际的)
2014年3月1日
研究完成 (实际的)
2014年3月1日
研究注册日期
首次提交
2012年8月13日
首先提交符合 QC 标准的
2012年8月14日
首次发布 (估计)
2012年8月17日
研究记录更新
最后更新发布 (实际的)
2019年3月5日
上次提交的符合 QC 标准的更新
2019年3月1日
最后验证
2019年3月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.