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Vitamin D Supplementation in Children With Sickle Cell Disease (VIDS)

2021年4月8日 更新者:College of Health Sciences、Makerere University

Effect of Vitamin D Supplementation on Sickle Cell Disease Hospitalisation and Related Complications Among Children in Mulago Hospital: A Randomised Clinical Trial

Children aged 6 months to 12 years of age will be randomised to receive vitamin D 60,000IU once a month for 3 months or a placebo. The vitamin D will be in form of granules supplied in sachets. The primary study outcomes will be incidence of hospitalisation and change in vitamin D levels following supplementation. Secondary outcomes will include incidence of vaso-occlusive crisis (VOC), acute severe respiratory illness, Vitamin D related Severe adverse events and requirements for blood transfusion

研究概览

详细说明

BACKGROUND: More than 75% of all children with sickle cell anemia (SCA) are born in sub-Saharan Africa annually. The hallmark of SCA is haemolytic anaemia and or pain crisis that often require hospitalisation. Interventions to reduce the complications, which are prerequisites for frequent hospitalisations, are needed urgently. Vitamin D deficiency is common in children with SCA and is associated with recurrent vaso-occlusive crisis, blood transfusion, hospitalisation and infections. Routine vitamin D supplementation is not practiced in the care of sickle cell disease patients yet it has been associated with improved bone health and bone mineral density, reduced chronic pain and improved quality of life.

HYPOTHESIS: Vitamin D supplementation will lead to a lower incidence of hospitalisation than placebo in Ugandan children with SCA.

METHODS: The study will be a randomized, placebo-controlled, double blind clinical trial in which 331 Ugandan children with SCA aged 6 months to 12 years inclusive will receive vitamin D (60,000IU granules monthly) and another 331 a placebo (identical to vitaminD in appearance) for 3 months. The primary study outcome will be incidence of hospitalisation. Secondary outcomes will include incidence of vaso-occlusive crisis (VOC), acute severe respiratory illness, Vitamin D related Severe adverse events and requirements for blood transfusion IMPACT: If this trial shows a reduction in hospitalisation, it will be the basis for a multi-site pre-post intervention clinical trial to assess real-world safety and efficacy of Vitamin D in African children with SCA. The monthly administration is easy, and since vitamin D is inexpensive, this trial has the potential to improve the health of hundreds/ thousands of African children with SCA through reduction of infection-related morbidity and mortality.

研究类型

介入性

注册 (预期的)

662

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。

学习联系方式

  • 姓名:Grace Ndeezi, PhD
  • 电话号码:+256 772453191
  • 邮箱:gndeezi@gmail.com

研究联系人备份

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

6个月 至 12年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Documented sickle cell disease (HbSS supported by hemoglobin electrophoresis results) attending Mulago Hospital Sickle Cell Clinic)
  2. Age range of 6 months to 12 years, inclusive, at the time of enrolment
  3. Weight at least 5.0 kg at the time of enrolment
  4. Willingness to comply with all study-related treatments, evaluations, and follow-up

Exclusion Criteria:

  1. Known other chronic medical condition (e.g., HIV, malignancy, Renal & liver disease, active clinical tuberculosis)
  2. Severe acute malnutrition determined by impaired growth parameters as defined by WHO weight for length/height less than -3SD.
  3. Evidence of Vitamin D supplementation in the past one month (by prescription or drug sample)

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:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
有源比较器:Vitamin D supplement
331 children will each received 60,000IU of vitamin D once a month for 3 months.
Vitamin D3 supplement
有源比较器:Intervention
The intervention arm will receive vitamin D3.
Vitamin D3 supplement

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
Frequency of hospitalisation among children with SCD supplemented with vitamin D versus placebo.
大体时间:3 months follow up
Number of children hospitalised during the follow up period and number of hospitalisations per child
3 months follow up
Effect of vitamin supplementation on serum levels of 25 Hydroxyvitamin D levels in children with SCD
大体时间:3 months follow up
Serum levels of 25 Hydroxyvitamin D
3 months follow up
Frequency of blood transfusion among children supplemented with vitamin D versus Placebo in children with sickle cell anaemia
大体时间:3 months follow up
The number of children requiring blood transfusion during follow up and the episodes per child
3 months follow up

次要结果测量

结果测量
措施说明
大体时间
Incidence of vaso-occlusive crises (VOC)
大体时间:3 months follow up
Incidence of painful vaso-occlusive crises
3 months follow up
Incidence of acute severe respiratory illnesses
大体时间:3 months follow up
Incidence of cough associated with difficult breathing confirmed as pneumonia or acute chest syndrome by a health worker
3 months follow up
Severe adverse events
大体时间:3 months follow up
Serious adverse events for example severe diarrhoea and vomiting with dehydration.
3 months follow up

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。

调查人员

  • 首席研究员:Grace Ndeezi, PhD、Makerere University, Kampala, Uganda

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 (预期的)

2021年5月17日

初级完成 (预期的)

2021年12月31日

研究完成 (预期的)

2022年1月31日

研究注册日期

首次提交

2020年12月4日

首先提交符合 QC 标准的

2020年12月9日

首次发布 (实际的)

2020年12月10日

研究记录更新

最后更新发布 (实际的)

2021年4月13日

上次提交的符合 QC 标准的更新

2021年4月8日

最后验证

2021年4月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

De-identified participant information may be shared with other researchers.

IPD 共享时间框架

within one year and the sharing period could extend beyond this period

IPD 共享访问标准

If requested by other researchers who have carried out similar studies for a meta-analysis

IPD 共享支持信息类型

  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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.

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