ISRCTN79220656暂停未知
High or low dose Syntocinon for induction of labour in nulliparous women: a double blind, randomised controlled trial
Birmingham Women’s and Children’s NHS Foundation Trust0 个研究点目标入组 2,400 人开始时间: 2021年5月20日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 暂停
- 发起方
- 入组人数
- 2,400
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
- 性别
- Female
入选标准
- •1. Nulliparous women at >24 +0/40 weeks gestation
- •2. Singleton cephalic pregnancy
- •3. Ruptured membranes undergoing induction of labour
- •4. Prescribed oxytocin is indicated as part of the induction process
- •5. Recieved prostin >6 h ago, or propess >30 min ago (if applicable)
- •6. Clinicians are willing to randomise
- •7. Give written informed consent to participate prior to randomisation
- •8. Aged =16 years
- •9. COVID-19 positive participants are eligible for study inclusion in accordance with local Trust/Health Board policy
排除标准
- •Nulliparous women who:
- •1. Are in the second stage of labour
- •2. Have any of the following conditions:
- •2.1. Existing cardiac disease
- •2.2. Bleeding disorders
- •2.3. Previous uterine surgery
- •2.4. Significant antepartum haemorrhage
- •3. Have a known contra-indication to oxytocin therapy
- •4. Are participating in other interventional trials of an Investigational Medicinal Product (IMP) or procedure for induction of labour
研究者
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