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临床试验/NCT04302428
NCT04302428已完成不适用

Zinc Status and Growth in Cystic Fibrosis

Indiana University1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2019年8月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
1
主要终点
Zinc Status

研究概览

简要总结

The purpose of this study is to improve the understanding of the relationship of zinc status and growth in infants and young children who were diagnosed with cystic fibrosis via newborn screening.

详细描述

The objective of this study is to improve the understanding of the relationship of zinc (Zn) status and growth in infant and young people with cystic fibrosis (PWCF). The investigators hypothesize that Zn deficiency in infant and young PWCF is associated with poor growth.

Aim #2: To study the association between Zn levels in red blood cells and nutritional status in PWCF at 3 months to 3 years of age and compare it to the association between serum Zn and nutritional status in the same population. Hypothesis: Lower Zn levels in red blood cells is associated with poorer nutritional status in infant and young PWCF and is a better measure of Zn status compared to serum Zn.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
3 Months 至 3 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients ages 3 months to 3 years with CF identified via new born screening

排除标准

  • History of meconium ileus
  • History of prematurity (born prior to completing 36 weeks 6 days gestation)

结局指标

主要结局

Zinc Status

时间窗: 1 day

Zn status in infant and young PWCF as measured by serum Zn and red blood cell Zn

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sarah Bauer

Assistant Professor, School of Medicine

Indiana University

研究点 (1)

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