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临床试验/NCT01751477
NCT01751477已完成不适用

Oral Probiotics (Infloran®) for Prevention of Necrotizing Enterocolitis in Very Low Birth Weight Infants

Medical University of Vienna2 个研究点 分布在 1 个国家目标入组 463 人开始时间: 2010年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
463
试验地点
2
主要终点
Incidence of NEC

研究概览

简要总结

Necrotizing enterocolitis (NEC) is one of the most devastating gastrointestinal emergencies in preterm neonates and a leading cause of death and morbidity.

The pathogenesis of NEC remains largely unclear, but it is widely considered as a multifactorial disease. Prematurity, enteral feeding, bacterial colonisation of the gut and intestinal ischemia have been proposed as major risk factors.

Probiotics may prevent NEC by improving the maturity and function of the gut mucosal barrier, modulating the immune system, promoting colonization of the gut with beneficial organisms and preventing colonization by pathogens.

A variety of clinical trials have evaluated the effect of different probiotic preparations on the occurrence of NEC in preterm infants. The results of recent metaanalyses suggest a benefit of probiotic bacteria in reducing the incidence of NEC and propose a change of practice.

The aim of the study is to evaluate the efficacy of the probiotic preparation Infloran® in reducing the incidence of NEC after implementation in clinical routine in preterm (< 34 weeks gestational age) very low birth weight infants compared to a historical cohort.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
— 至 7 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Neonates admitted to the neonatal intensive care unit on day 1 of life
  • Very low birth weight (<1500 gram)
  • Prematurity < 34/0 weeks gestational age
  • For group receiving probiotics: 230 infants born after the 20/Sep/2010 (i.e. date of introduction of Infloran in clinical routine)
  • For control group (historical): 230 infants born before 2010

排除标准

  • Malformation of the gut (omphalocele, gastroschisis, intestinal atresia)
  • Death before seven days of life, except due to NEC
  • Transfer to another hospital before 37 weeks of corrected gestational age, except those who were transferred to a partner clinic using the same protocol for probiotic supplementation
  • For group receiving probiotics: Infants who did not receive Infloran® starting in the first week of life or stopped before 34 weeks gestational age, except infants who developed NEC (reason for discontinuation of Infloran)

结局指标

主要结局

Incidence of NEC

时间窗: From birth to 37 weeks of gestational age (usually around 12 weeks)

NEC stages 2 or 3 according to Bell´s modified staging of NEC

次要结局

  • Severity of NEC(From birth to 37 weeks of gestational age (usually around 12 weeks))
  • Influence of enteral feeding with human milk or formula on the incidence of NEC after the implementation of Infloran®(From birth to 37 weeks of gestational age (usually around 12 weeks))

研究者

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

Andreas Repa

MD

Medical University of Vienna

研究点 (2)

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