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临床试验/NCT01756040
NCT01756040已完成1 期

Gut Permeability in Very Low Birth Weight Infants

University of Maryland, Baltimore1 个研究点 分布在 1 个国家目标入组 211 人开始时间: 2013年2月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
211
试验地点
1
主要终点
Intestinal Permeability

研究概览

简要总结

Necrotizing enterocolitis (NEC) is a life-threatening, gastrointestinal emergency characterized by increased intestinal permeability, affects approximately 7 to 10% of infants <1500 g birthweight, and typically occurs within 7 to 14 days of birth. Mortality is as high as 30-50%. Prematurity is the greatest risk factor for the development of NEC due to the physiological immaturity of the gastrointestinal tract and altered or abnormal gut microbiota. Several studies have demonstrated that the initiation of an intense systemic and local inflammatory cascade leads to intestinal necrosis. The human intestine is lined by a single layer of cells exquisitely responsive to multiple stimuli and is populated by a complex climax community of microbial partners. Under normal circumstances, these intestinal cells form a tight but selective barrier to "friends and foes": microbes and most environmental substances are held at bay, but nutrients are absorbed efficiently. Epithelial barrier integrity is itself dynamic and matures over time starting soon after birth, though the mechanisms regulating dynamic permeability are poorly understood. Low birth weight, prematurity, and early postnatal age are associated with a leaky gut. Although intestinal permeability is higher at birth in preterm than term infants, there is usually rapid maturation of the intestinal barrier over the first few days of life in both populations. The investigators hypothesize that increased levels of measures of intestinal permeability (urine lactulose/rhamnose (LA/Rh), and fecal alpha1- antitrypsin will identify infants at high risk for NEC and that intestinal probiotic strains will be associated with intestinal barrier maturation. The purpose of the study is to determine whether clinical factors in combination with non-invasive stool test such as antitrypsin (A1AT) and microbiota composition profile are associated with intestinal permeability determined by excretion of non-metabolized sugar probes in urine (LA/Rh ratio). These studies may lead to a non-invasive screening test to identify preterm infants at risk for NEC.

详细描述

The proposed study will evaluate the intestinal permeability measured by the urinary La/Rh ratio at one timepoint between d7-10 of life in 200 preterm infants 24-32 weeks gestation in preparation for a future study of probiotics to improve intestinal permeability in this population.

Primary Objective: To estimate mean and variance in IP measured by urinary Lactulose/Rhamnose ratio at 7-10d of life in neonates born between 24 and 32 weeks of gestational age.

Secondary Objectives

  1. To assess stool microbiome characteristics in association with intestinal permeability in preterm infants measured by the urinary lactulose/rhamnose ratio.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

年龄范围
— 至 4 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Gestational age 24-32 weeks
  • Exclusion criteria:
  • Nonviable or planned withdrawal of care
  • Significant GI dysfunction (e.g. heme-positive stools, abdominal distension (girth >2 cm baseline), or bilious emesis/aspirates.
  • Triplet or higher order multiple
  • Severe asphyxia
  • Lethal chromosome abnormalities
  • Cyanotic congenital heart disease
  • Intestinal atresia or perforation
  • Abdominal wall defects
  • Known galactosemia or other galactose intolerance

排除标准

  • 未提供

研究组 & 干预措施

Lactulose - rhamnose solution

Other

Preterm Infants age 24-32 weeks gestation

干预措施: Lactulose -rhamnose solution (Drug)

结局指标

主要结局

Intestinal Permeability

时间窗: 7-10 days postnatal

Intestinal Permeability measured by urinary excretion of orally administered lactulose/rhamnose (La/Rh ratio)

次要结局

  • Breastmilk Feeding Duration Prior to La/Rh Measurement(7-10 days postnatal)
  • Stool Microbiota Relative Abundance(7-10 days postnatal)
  • Stool Alpha-1 Antitrypsin(7-10 days postnatal)

研究者

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

Rose Viscardi

University of Maryland

University of Maryland, Baltimore

研究点 (1)

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