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Vitamin D and Vascular Health in Children

2020年6月10日 更新者:Kumaravel Rajakumar、University of Pittsburgh

Vitamin D and Vascular Function in Obese Children

In this study, we will test the central hypothesis that enhancement of vitamin D status in obese and overweight children will improve their vascular health and their cardiovascular disease (CVD) and metabolic syndrome risk profile.

研究概览

地位

完全的

详细说明

Our primary objective is to determine, in obese and overweight children aged 10 to 18 years with vitamin D deficiency (defined as serum 25-hydroxyvitamin D <20 ng/mL), the efficacy of enhanced vitamin D3 supplementation in improving vascular endothelial function, arterial stiffness, insulin sensitivity, and metabolic syndrome risk status; and to assess whether these effects are dose-dependent. As a secondary objective, we will examine the vitamin D supplementation-induced effect on adipokines and inflammatory markers relevant to CVD risk. In a double-masked, controlled trial, we will randomize 252 eligible children to receive either 600 IU (conventional supplementation), or 1000 IU or 2000 IU (enhanced supplementation) of vitamin D3 daily for 6 months.

In terms of reporting of results, the following pre-specified outcomes are included in the primary manuscript (PubMed PMID:31950134 -- see Reference section for citation details)

  1. Waist Circumference
  2. Serum High Density Lipoprotein (HDL) Cholesterol
  3. Serum Triglycerides
  4. Inflammatory markers (Plasma TNF-alpha, high-sensitivity C-reactive protein, and IL-6)
  5. Adiopkines (Plasma Leptin and Adiponectin)

Plasma nitric oxide metabolites were not measured.

研究类型

介入性

注册 (实际的)

225

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

    • Pennsylvania
      • Pittsburgh、Pennsylvania、美国、15213
        • Primary Care Center, Children's Hospital of Pittsburgh of UPMC

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

10年 至 18年 (孩子、成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Eligible subjects will be 10 to 18 years of age;
  • obese or overweight (BMI ≥85th %tile);
  • otherwise healthy, and
  • have a serum 25(OH)D concentration <20 ng/mL

Children taking multivitamins should be able to hold off their multivitamins during the course of the study.

Exclusion Criteria:

Children will be excluded if they

  • (a) have hepatic or renal disease, metabolic rickets, malabsorptive disorders, primary hyperparathyroidism, hyperthyroidism, or other chronic disorders that could affect vitamin D metabolism;
  • (b) are receiving treatment with anticonvulsants, systemic glucocorticoids, pharmacologic doses of vitamin D (≥1000 IU of vitamin D2 or D3 daily), antihypertensives, vasoactive drugs, antilipidemics, metformin, antipsychotics, or other oral insulin regulators;
  • (c) have cholelithiasis or urolithiasis;
  • (d) have type 1 or type 2 diabetes; or
  • (e) have a condition or underlying abnormality that could compromise the safety of the subject.

Post-menarchial girls with a positive pregnancy test at randomization, or subjects found during the screening phase to have hypercalcemia (serum calcium >10.8 mg/dL) or significant fasting hyperglycemia (fasting blood glucose ≥ 125 mg/dL) will also be excluded.

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 D3 2000 IU
Vitamin D3 2000 IU tablet once daily by mouth for 6 months
Tablet form
其他名称:
  • 胆钙化醇
有源比较器:Vitamin D3 1000 IU
Vitamin D3 1000 IU tablet by mouth once daily for 6 months
Tablet form
其他名称:
  • 胆钙化醇
安慰剂比较:Vitamin D3 600 IU
Vitamin D3 600 IU tablet by mouth once daily for 6 months
Tablet form
其他名称:
  • 胆钙化醇

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
Flow-mediated Dilation (FMD) Percentage
大体时间:6 months
Brachial artery flow-mediated dilation percentage is a measure of endothelial function. FMD percentage calculation is based on baseline brachial artery diameter(brachialADbase) and change in brachial artery diameter (brachialADchange) during post-occlusive reactive hyperemia. FMD% was determined using the formula (brachialADchange/brachialADbase) x 100.
6 months

次要结果测量

结果测量
措施说明
大体时间
Pulse-wave Velocity (PWV)
大体时间:6 months
PWV is a measure of arterial stiffness. Higher values of PWV indicate greater degree of arterial stiffness.
6 months
Augmentation Index at Heart Rate of 75 Beats/Min (AIx-75)
大体时间:6 months

AIx-75 is a measure of arterial stiffness. AIx was measured through radial arterial tonometry using SphygmoCor.

Radial pulse waveform are analyzed through an automatic software function to determine aortic pulse waveform and aortic or central systolic (cSBP) and diastolic blood pressure (cDBP), and these measurements are further analyzed automatically to calculate AIx.

AIx is a composite measure of the magnitude of wave reflection and arterial stiffness in all conduit arteries which affect the timing of the wave reflection. AIx = P2-P1/cSBP-cDBP, where P1 is the height of the incident pressure wave form during systole, P2 is the height of the reflected wave added to the incident wave, cSBP is the aortic systolic BP, and cDBP is the aortic diastolic BP. AIx adjusted to heart rate of 75 beats/min (AIx-75) is a validated index of arterial stiffness, with higher values indicating higher degree of arterial stiffness.

6 months
Central Systolic Blood Pressure
大体时间:6 months
a measure of cardiometabolic health
6 months
Central Diastolic Blood Pressure
大体时间:6 months
a measure of cardiometabolic health
6 months
Systemic Systolic Blood Pressure
大体时间:6 months
a measure of cardiometabolic health
6 months
Systemic Diastolic Blood Pressure
大体时间:6 months
a measure of cardiometabolic health
6 months
Fasting Blood Glucose
大体时间:6 months
a measure of cardiometabolic health
6 months
1/Fasting Insulin Ratio
大体时间:6 months
1/fasting insulin ratio is a measure of insulin sensitivity. Increases in 1/fasting insulin ratio indicate improvements in insulin sensitivity.
6 months

其他结果措施

结果测量
措施说明
大体时间
Body Mass Index (BMI)
大体时间:6 months
a surrogate measure of adiposity
6 months

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:Kumaravel Rajakumar, MD, MS、University of Pittsburgh, Children's Hospital of Pittsburgh of UPMC

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 (实际的)

2013年8月1日

初级完成 (实际的)

2018年8月13日

研究完成 (实际的)

2018年8月13日

研究注册日期

首次提交

2013年2月20日

首先提交符合 QC 标准的

2013年2月20日

首次发布 (估计)

2013年2月22日

研究记录更新

最后更新发布 (实际的)

2020年6月24日

上次提交的符合 QC 标准的更新

2020年6月10日

最后验证

2020年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • PRO12100034
  • R01HL112985 (美国 NIH 拨款/合同)
  • 5R01HL112985-05 (美国 NIH 拨款/合同)

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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