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Supply With Micronutrients (Purine and Pyrimidine) in Infants: a Prospective and Observational Study

2020年9月16日 更新者:University Hospital Tuebingen

Beobachtungsstudie Zur Versorgung Reif- Und Frühgeborener Mit ausgewählten Mikronährstoffen Wissenschaftliche Untersuchung Bei Minderjährigen

Concentrations of micronutrients (especially purine and pyrimidine) in cord blood, blood of mothers and infants and human milk is studied

研究概览

详细说明

Collection of:

  1. cord plasma in preterm and term infants.
  2. remnants of clinically indicated blood samples of mothers 24 hours before or after birth.
  3. remnants of clinically indicated blood samples of preterm and term infants during neonatal care.
  4. breast milk once a weak during neonatal care of the infant.

Determination concentrations of micronutrients by mass spectrometry.

Aim is to compare cord plasma concentrations with postnatal plasma concentrations and to measure concentrations in breast milk to determine the actual supply.

Update September 2020:

The results obtained according to the original protocol revealed a serious sample instability when using remnants of clinical blood samples. Remnants can not be used and therefore the protocol had to be changed. A new approval of the Ethics Committee was obtained and is available to the study team. The following changes for sample collection were implemented: an additional blood sample (2.7ml EDTA blood) is taken from the mothers after approval.The blood samples of premature and newborns (max. 3x 0.2 ml) are obtained when a clinically indicated blood sample is taken. In both cases the serum is frozen immediately within one hour after collection.

Due to these changes, the expected end of the study is postponed to 2021.

研究类型

观察性的

注册 (预期的)

150

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

      • Tuebingen、德国、72076
        • 招聘中
        • University Children's Hospital Tuebingen
        • 接触:
        • 首席研究员:
          • Axel Franz, MD

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

1秒 至 6个月 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

infants and preterm infants

描述

Inclusion Criteria:

  • 23+0-42+6 SSW

Exclusion Criteria:

  • congenital malformation, genetic disorders
  • metabolic disease of the infant
  • missing agreement

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

队列和干预

团体/队列
干预/治疗
23-27w
preterm infants 23+0-27+6SSW
collection of cord blood
collection of remnant of clinically indicated blood sample
collection of remnant of clinically indicated blood sample. If not available blood sample is taken after mother agreed
collection of breast milk 1/week during neonatal care (maximum 8 weaks)
28-31w
preterm infants 28+0-31+6SSW
collection of cord blood
collection of remnant of clinically indicated blood sample
collection of remnant of clinically indicated blood sample. If not available blood sample is taken after mother agreed
collection of breast milk 1/week during neonatal care (maximum 8 weaks)
32-34w
preterm infants 32+0 - 34+6SSW
collection of cord blood
collection of remnant of clinically indicated blood sample
collection of remnant of clinically indicated blood sample. If not available blood sample is taken after mother agreed
collection of breast milk 1/week during neonatal care (maximum 8 weaks)
35-36w
preterm infants 35+0-36+6 SSW
collection of cord blood
collection of remnant of clinically indicated blood sample
collection of remnant of clinically indicated blood sample. If not available blood sample is taken after mother agreed
collection of breast milk 1/week during neonatal care (maximum 8 weaks)
37-42w
term infants 37+0-42+6
collection of cord blood
collection of remnant of clinically indicated blood sample
collection of remnant of clinically indicated blood sample. If not available blood sample is taken after mother agreed
collection of breast milk 1/week during neonatal care (maximum 8 weaks)

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Concentration of purine and pyrimidine in cord plasma
大体时间:at birth
at birth

次要结果测量

结果测量
大体时间
Concentration of purine and pyrimidine in neonatal plasma
大体时间:at times when a clinically indicated blood sample is taken before discharge home from the initial neonatal hospitalization (at a postnatal age of up to 4-5 months at the most in very preterm infants)
at times when a clinically indicated blood sample is taken before discharge home from the initial neonatal hospitalization (at a postnatal age of up to 4-5 months at the most in very preterm infants)
Concentration of purine and pyrimidine in breast milk
大体时间:once a week before discharge home from the initial neonatal hospitalization, maximum 8 weeks
once a week before discharge home from the initial neonatal hospitalization, maximum 8 weeks
Concentration of purine and pyrimidine in plasma of mothers
大体时间:24 hours before and after birth
24 hours before and after birth

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。

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)

2017年3月1日

初级完成 (预期的)

2021年10月1日

研究完成 (预期的)

2021年10月1日

研究注册日期

首次提交

2018年5月9日

首先提交符合 QC 标准的

2018年5月9日

首次发布 (实际的)

2018年5月22日

研究记录更新

最后更新发布 (实际的)

2020年9月18日

上次提交的符合 QC 标准的更新

2020年9月16日

最后验证

2020年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • NEO-MICRO

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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

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