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临床试验/NCT00182312
NCT00182312已完成3 期

Efficacy and Safety of Methylxanthines in Very Low Birthweight Infants

McMaster University66 个研究点 分布在 9 个国家目标入组 2,000 人开始时间: 1999年10月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
2,000
试验地点
66
主要终点
combined rate of mortality and neurodevelopmental disability in survivors at a corrected age of 18 months.

研究概览

简要总结

At least 5 of every 1000 live-born babies are very premature and weigh only 500 to 1250 grams at birth. Approximately 30-40% of these high-risk infants either die or survive with lasting disabilities. The aim of this research is to reduce this heavy burden of illness. A multi-center randomized controlled trial has been designed in which 2000 very low birth weight infants will be enrolled. Our goal is to determine whether the avoidance of methylxanthine drugs will improve survival without disability to 18 months, corrected for prematurity.

Methylxanthine drugs such as caffeine are used to prevent or treat periodic breathing and breath-holding spells in premature infants. However, there is a striking lack of evidence for the long-term efficacy and safety of this therapy. Methylxanthines block a naturally occurring substance, called adenosine, which protects the brain during episodes of oxygen deficiency. Such episodes are common in infants who are treated with methylxanthines. It is possible that methylxanthines may worsen the damage caused by lack of oxygen. Therefore, this trial will clarify whether methylxanthines cause more good than harm in very low birth weight infants.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
— 至 10 Days(Child)
性别
All
接受健康志愿者

入选标准

  • birthweight 500 to 1250 grams
  • postnatal age day 1 to day 10
  • infant considered a candidate for methylxanthine therapy by clinical staff

排除标准

  • dysmorphic features or congenital malformations that adversely affect life expectancy or neurodevelopment
  • unlikely to comply with long-term follow-up
  • prior treatment with a methylxanthine

结局指标

主要结局

combined rate of mortality and neurodevelopmental disability in survivors at a corrected age of 18 months.

时间窗: corrected age of 18 months

次要结局

  • bronchopulmonary dysplasia(discharge home)
  • necrotizing enterocolitis(discharge home)
  • brain injury: intra- and periventricular hemorrhage, periventricular leucomalacia and/or ventriculomegaly(discharge home)
  • retinopathy of prematurity(discharge home)
  • growth failure(corrected age of 18 months)
  • functional status at 5 years and at 11-12 years(corrected age of 5 years and chronological age of 11-12 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (66)

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