NCT00391339Unknown2 期
Bryophyllum p. Versus Nifedipine for the Treatment of Premature Contractions
适应症
相关药物
试验速览
- 阶段
- 2 期
- 发起方
- Weleda AG
- 入组人数
- 140
- 试验地点
- 2
研究概览
简要总结
In a prospective, randomised study the efficacy and tolerability of bryophyllum p. (p.o) vs. nifedipine (p.o) will be proofed in a defined group of pregnant women with threatened preterm labour.
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
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •Bishop Score > 5
研究者
研究点 (2)
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