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临床试验/NCT02552706
NCT02552706Unknown不适用

The Efficacy and Mechanisms of Oral Probiotics in Preventing Necrotizing Enterocolitis Among Very Low Birth Weight Infants With Formula-feeding

Shenzhen Bao'an Maternal and Child Health Hospital4 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2014年9月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
270
试验地点
4
主要终点
the incidence of combined death and necrotizing enterocolitis

研究概览

简要总结

The purpose of this study is to investigate the efficacy and its mechanisms of oral mixture probiotics in preventing necrotizing enterocolitis among the preterm very low birth weight infants.

详细描述

Necrotizing enterocolitis (NEC) remains the most catastrophic gastrointestinal emergencies in preterm very low birth weight (VLBW) infants.Although study showed it is a multifactorial disease, its pathogenesis is still not yet unclear currently. Prematurity and formula feeding is considered as the main risk factors.Gut microbiota disturbance and immature immune system is associated with NEC. A lot of studies had showed that oral probiotics can alter gut microbiota flora colonization and reduce the incidence of NEC,but the exact mechanism remains unclear.The aim of this study is to elucidate the clinical efficacy and possible molecular mechanism of oral mixture probiotics in preventing NEC among preterm VLBW infants.

Patient Registry procedures: First,randomized numbers was generated by the computer and sent to the principal investigator(PI) at each center when an infant was eligible for enrollment.Second, patient will be assigned randomly to experimental group or control group by PI.Finally,the PI at each center will be responsible for the accuracy,completeness or representativeness of medical records, registry forms,data collection.

Sample size determination: The incidence of death and NEC was around 20% recently.To reduce the incidence of NEC and death to 10% at discharge would require a 50% improvement.At 80% power at P = 0.05 (two-sided),the loss rate of 0.2, this would require 135 subjects per arm.

Statistical analysis

The two groups were compared by a Χ2-test for categorical variables,Mann-Whitney U Test were used when reporting medians.A P value of <0.05 was considered statistically significant.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
— 至 3 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Preterm infants ≦ 34 weeks gestational age and birth weight below 1500 gm and who survive to NICU are eligible for the trial.

排除标准

  • severe asphyxia (stage III),
  • fetal chromosomal anomalies,
  • cyanotic congenital heart disease,
  • congenital intestinal atresia, gastroschisis, omphalocele, active upper gastric intestinal bleeding,
  • lacking/refused of parental consent,
  • those who are fasted for >3 weeks during the study period.

结局指标

主要结局

the incidence of combined death and necrotizing enterocolitis

时间窗: at 36 weeks correct gestational age

次要结局

  • the incidence of sepsis,intraventricular hemorrhage(IVH)(grade 3-4),feeding intolerance(FI),bronchopulmonary dysplasia(BPD),parenteral nutrition associated liver disease(PNALD)and retinopathyof prematurity(ROP).(participants will be followed for the duration of hospital stay, an expected average of 8 weeks)

研究者

发起方
Shenzhen Bao'an Maternal and Child Health Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

liyuefeng

Ward chief of department of neonatology

Shenzhen Bao'an Maternal and Child Health Hospital

研究点 (4)

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