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临床试验/NCT00518856
NCT00518856已完成不适用

Lufwanyama Neonatal Survival Project

Boston University0 个研究点目标入组 3,559 人开始时间: 2006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
3,559
主要终点
mortality

研究概览

简要总结

We seek to determine whether we can reduce day 28 mortality in Zambian newborns by training traditional birth attendants a modified version of the neonatal resuscitation protocol (NRP) and by improving their abiltiy to identify sepsis and initiate antibiotics in the field.

详细描述

This is a cluster randomized trial of the impact of providing additional training and supplies to traditional birth attendants in a rural setting in Zambia. 120 TBAs are randomized into intervention/control. Intervention TBAs receive NRP training, supplies for neonatal resuscitation, receiving blankets for thermoregulation, and amoxicillin tablets. Control TBAs continue according to prior standard of care. Primary outcome is mortality at 28 days life as a proportion of births attended by TBAs in each study arm.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • TBA trained in safe delivery;
  • willing to sign informed consent; willing to be randomized; willing to adhere to study procedures

排除标准

  • TBA living outside of Lufwanyama district

结局指标

主要结局

mortality

时间窗: day 28

次要结局

  • perinatal mortality(day zero)
  • sepsis mortality(deaths between days 1-28)
  • cost effectiveness(days 0-28)
  • successful delivery of nevirapine prophylaxis to HIV exposed deliveries(day zero umbilical cord dried blood spot)

研究者

申办方类型
Other

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