临床试验/NCT00760942

NCT00760942已完成不适用

Randomized Study of a Liquid High-Calorie Preterm Formula Versus Powdered Human Milk Fortifier in Very-Low Birthweight Infants

University of Oklahoma1 个研究点分布在 1 个国家目标入组 84 人开始时间: 2008年10月1日最近更新: 2013年12月10日

适应症

干预措施

试验速览

阶段: 不适用
状态: 已完成
发起方: University of Oklahoma
入组人数: 84
试验地点: 1
主要终点: The primary outcome will be weight gain in g/kg/d over the observation period. Body weight will be measured daily.

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study aims to compare the short-term effects on growth and feeding tolerance of a liquid high calorie formula added to human milk versus powdered human milk fortifier in small preterm infants.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Supportive Care
盲法: None

入排标准

年龄范围: 1 Day 至 10 Weeks（Child）
性别: All
接受健康志愿者: 否

入选标准

•Infants between 500 and 1499 grams of birthweight, receiving mother's milk.

排除标准

•Infants with major congenital anomalies and previous history of gastrointestinal disease.

研究组 & 干预措施

1

Active Comparator

Liquid human milk fortifier

干预措施: Similac special care 30 (Dietary Supplement)

2

Active Comparator

Powdered human milk fortifier

干预措施: Similac human milk fortifier (Dietary Supplement)

结局指标

主要结局

The primary outcome will be weight gain in g/kg/d over the observation period. Body weight will be measured daily.

时间窗: 2 - 6 weeks

次要结局

Hospital stay and feeding intolerance(2-6 weeks)

研究者

发起方

University of Oklahoma

申办方类型

Other

责任方

Sponsor

研究点 (1)

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