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临床试验/NCT03663556
NCT03663556Unknown不适用

Feeding the Preterm Gut Microbiota - Impact of Infant-feeding on Preterm Gut Microbiota Development

Universidade do Porto2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年5月25日最近更新:
适应症

试验速览

阶段
不适用
入组人数
60
试验地点
2
主要终点
Changes from baseline intestinal microbiota composition of preterm infants in relation to infant-feeding profile (breast milk, donor human milk or formula) at 7,14 and 21 days.

研究概览

简要总结

Preterm infants are especially vulnerable to gut microbiota disruption and dysbiosis since their early gut microbiota is less abundant and diverse. Several factors may influence infants' microbiota such as mother's diet, mode of delivery, antibiotic exposure and type of feeding. The main goal of this observational study is to evaluate the impact of different types of feeding (breast milk, donor human milk and preterm formulas) on the intestinal microbiota of preterm infants hospitalized in the neonatal intensive care unit (NICU) of Maternidade Alfredo da Costa (MAC). Furthermore, the influence of mode of delivery and the mother's diet, among others factors, on vertical microbiota transmission will be evaluated. After delivery, mothers will be asked to collect their own fecal samples and will be invited to complete a semi-quantitative food frequency questionnaire. Stool samples will be collected from premature infants every 7 days. DNA will be extracted from fecal samples and different bacterial genus and species will be analyzed.

详细描述

Meconium and the additional 3 fecal samples will be collected from preterm infants by the nursing team of MAC Neonatology Unit. Fecal samples will be collected every 7 days, during 21 days, from diapers into sterile tubes. Mothers will be asked to collect their own fecal samples with an appropriate stool collection kit (EasySampler®) and will be invited to complete a semi-quantitative food frequency questionnaire, previously validated for the Portuguese population.

Infant-feeding profile (breast milk, donor human milk or formula) of preterm infants will be recorded every day to select the most representative (>50 %) type of infant-feeding received during the 7 days prior to each fecal sample collection.

Additionally, detailed clinical data will be collected during the preterm infant enrollment in the study. Personal clinical data includes sociodemographic information and clinical intrapartum and postpartum outcomes, such as newborn's weight, days of antibiotic exposure, number of total days of hospitalization and others outcomes related to the preterm clinical evolution.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
— 至 2 Days(Child)
性别
All
接受健康志愿者

入选标准

  • To be eligible for enrolment, preterm infants must have been admitted to the NICU in less than 24 hours of life, have been born with less than 32 weeks with absence of malformations or metabolic diseases.

排除标准

  • non applicable

结局指标

主要结局

Changes from baseline intestinal microbiota composition of preterm infants in relation to infant-feeding profile (breast milk, donor human milk or formula) at 7,14 and 21 days.

时间窗: Infant-feeding type of preterm infants before the first, second, third and fourth collection will be recorded during these 21 days.

Infant-feeding profile (breast milk, donor human milk or formula) will be recorded every day to select the most representative type of infant-feeding (\> 50 %) received during the 7 days prior to each fecal sample collection.

Changes from baseline intestinal microbiota composition of preterm infants at 7, 14 and 21 days.

时间窗: The first fecal sample (meconium) of preterm infants will be collected. Afterwards, fecal samples will be collected every 7 days, during 21 days.

The intestinal microbiota profile of preterm infants will be evaluated over time.

次要结局

  • Changes in maternal gut microbiota in relation to clinical variables described below(Clinical variables will be collected daily, until study completion an average of 2 years.)
  • Maternal intestinal microbiota composition, analyzed by RT-PCR.(Maternal fecal samples will be collected after delivery up to 1 week.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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