Rapid normalization of vitamin D deficiency in PICU (VITdALIZE-KIDS): study protocol for a phase III, multicenter randomized controlled trial.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Katie O'Hearn, Kusum Menon, Lisa Albrecht, Karin Amrein, Philip Britz-McKibbin, Florence Cayouette, Karen Choong, Jennifer Ruth Foster, Dean A Fergusson, Alejandro Floh, Patricia Fontela, Pavel Geier, Elaine Gilfoyle, Gonzalo Garcia Guerra, Anna Gunz, Erick Helmeczi, Ali Khamessan, Ari R Joffe, Laurie Lee, Lauralyn McIntyre, Srinivas Murthy, Simon J Parsons, Tim Ramsay, Lindsay Ryerson, Marisa Tucci, Dayre McNally
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引用次数: 0

Abstract

Background: The rate of vitamin D deficiency (VDD) in critically ill children worldwide has been estimated at 50%. These children are at risk of multiple organ dysfunction, chronic morbidity, and decreased health related quality of life (HRQL). Pediatric and adult ICU clinical trials suggest that VDD is associated with worse clinical outcomes, although data from supplementation trials are limited and inconclusive. Our group's phase II multicenter dose evaluation pilot study established the efficacy and safety of an enteral weight-based cholecalciferol loading dose to rapidly restore vitamin D levels in critically ill children.

Methods: Our aim is to evaluate the impact of this dosing regimen on clinical outcomes. VITdALIZE-KIDS is a pragmatic, phase III, multicenter, double-blind RCT aiming to randomize 766 critically ill children from Canadian PICUs. Participants are randomized using a 1:1 scheme to receive a single dose at enrollment of enteral cholecalciferol (10,000 IU/kg, max 400,000 IU) or placebo. Eligibility criteria include critically ill children aged newborn (> 37 weeks corrected gestational age) to < 18 years who have blood total 25-hydroxyvitamin D < 50 nmol/L. The primary objective is to determine if rapid normalization of vitamin D status improves HRQL at 28 days following enrollment. The secondary objective is to evaluate the impact of rapid normalization of vitamin D status on multiple organ dysfunction. The study includes additional tertiary outcomes including functional status, HRQL and mortality at hospital discharge and 90 days, PICU and hospital length of stay, and adverse events related to vitamin D toxicity. Additionally, we are performing comprehensive vitamin D speciation and non-targeted metabolite profiling as part of a sub-study for the first 100 participants from whom an enrollment and at least one post-intervention blood and urine sample were obtained.

Discussion: The VITdALIZE-KIDS trial is the first phase III, multicenter trial to evaluate whether rapid normalization of vitamin D status could represent a simple, inexpensive, and safe means of improving outcomes following pediatric critical illness. Recruitment was initiated in June 2019 and is expected to continue to March 2026.

Trial registration: Clinicaltrials.gov, NCT03742505. Study first submitted on November 12, 2018 https://clinicaltrials.gov/study/NCT03742505.

儿童重症监护病房维生素 D 缺乏症快速恢复正常(VITdALIZE-KIDS):III 期多中心随机对照试验研究方案。
背景:据估计,全球重症儿童的维生素 D 缺乏率(VDD)为 50%。这些儿童有可能出现多器官功能障碍、慢性发病和与健康相关的生活质量下降(HRQL)。儿童和成人重症监护室的临床试验表明,VDD 与较差的临床预后有关,但补充试验的数据有限,且尚无定论。我们小组的 II 期多中心剂量评估试验研究确定了基于体重的肠道胆钙化醇负荷剂量对快速恢复重症儿童维生素 D 水平的有效性和安全性:我们的目的是评估这种给药方案对临床结果的影响。VITdALIZE-KIDS 是一项务实的 III 期多中心双盲 RCT 研究,旨在对来自加拿大 PICU 的 766 名重症儿童进行随机分组。参与者按照 1:1 的比例随机分配,在入院时接受单剂量肠内胆钙醇(10,000 IU/kg,最大剂量 400,000 IU)或安慰剂。资格标准包括新生儿(胎龄大于 37 周)至讨论期的重症患儿:VITdALIZE-KIDS试验是首个III期多中心试验,旨在评估快速使维生素D状态正常化是否是一种简单、廉价、安全的改善儿科危重病后预后的方法。招募工作于2019年6月启动,预计将持续到2026年3月:Clinicaltrials.gov, NCT03742505.研究首次提交于2018年11月12日https://clinicaltrials.gov/study/NCT03742505。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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