2024-511848-55-00招募中3 期
A double-blind randomized placebo-controlled four-arm trial to assess the efficacy of oral bicarbonate and intravenous butylscopolamine bromide to facilitate spontaneous (non-operative) delivery in pregnant female participants with induction of labor.
Oslo University Hospital HF10 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2024年10月9日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 3,000
- 试验地点
- 10
- 主要终点
- Spontaneous vs operative delivery. Operative delivery defined as cesarean delivery, vacuum or forceps
研究概览
简要总结
To assess the efficacy of oral bicarbonate and intravenous butylscopolamine bromide to facilitate spontaneous (non-operative) delivery in pregnant female participants with induction of labor.
入排标准
- 年龄范围
- 18 years 至 64 years（18-64 Years）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Nulliparous women with induction of labor. Singleton fetus in cephalic presentation at term
排除标准
- •Spontaneous start of labor. Multifetal pregnancy. Known intolerance to study medications. Preterm birth.
结局指标
主要结局
Spontaneous vs operative delivery. Operative delivery defined as cesarean delivery, vacuum or forceps
Spontaneous vs operative delivery. Operative delivery defined as cesarean delivery, vacuum or forceps
次要结局
未报告次要终点
研究者
Trond
Scientific
Oslo University Hospital HF
研究点 (10)
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