NCT00185952已完成不适用
Nifedipine for the Maintenance Tocolysis of Preterm Labor: Comparison to Placebo in a Prospective, Randomized Double Blind Trial
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- Achieving 37 weeks gestation
研究概览
简要总结
Comparing nifedipine to placebo for the maintenance tocolysis of preterm labor
详细描述
To estimate whether maintenance nifedipine tocolysis after arrested preterm labor prolongs pregnancy and improves neonatal outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •arrested preterm labor
排除标准
- •ruptured membranes, fetal distress, placenta previa, placental abruption, maternal medical contraindication to tocolysis
研究组 & 干预措施
Nifedipine
Active Comparator
Maintenance tocolysis with nifedipine.
干预措施: Nifedipine (Drug)
Placebo
Placebo Comparator
Maintenance tocolysis with placebo tablets.
干预措施: Nifedipine (Drug)
结局指标
主要结局
Achieving 37 weeks gestation
时间窗: delivery
次要结局
- Incidence of recurrent preterm labor(Delivery)
- Neonatal outcomes(Discharge of neonate)
研究者
研究点 (1)
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