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临床试验/IRCT201402072624N11
IRCT201402072624N11已完成3 期

A comparison between the effect of the two methods of 12 versus 24 hours interval of betamethasone administration on neonatal respiratory distress syndrome in women with preterm labor.distress syndrome.

Vice chancellor for research ,Iran University of Medical Sciences.0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • singleton pregnancy and gestational age of 26-34 weeks.
  • Exclusion criteria: known allergy for betamethazone; history of any known maternal systemic disorders like hypertension, diabetes, liver and cardiac disease, renal failure and neoplasia.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research ,Iran University of Medical Sciences.

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