ISRCTN99841044已完成3 期
High Or Low Dose Syntocinon® for delay in labour: the HOLDS trial
Birmingham Womens NHS Foundation Trust0 个研究点目标入组 1,500 人开始时间: 2016年8月3日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1,500
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 with singleton cephalic pregnancy at term (37-42 weeks gestation)
- •2. Confirmed delay in labour and ruptured membranes for whom the clinical decision has been made to prescribe Syntocinon for augmentation of labour
- •According to NICE guidance [NICE 2014], labour is established when there are regular painful contractions and progressive cervical dilation from 4 cm. Delay is suspected when cervical dilation of < 2 cm in 4 hours occurs once labour is established. Delay is confirmed when progress of <1 cm in 2 hours is found on repeat vaginal examination.
排除标准
- •1. Multiparous women
- •2. Nulliparous women who:
- •2.1. Are undergoing induction of labour
- •2.2. Have a BMI >40 at booking
- •2.3. Have a multiple pregnancy
- •2.4. Have existing cardiac disease, bleeding disorders, diabetes (either pre-existing or gestational), previous uterine surgery
- •2.5. Have had significant antepartum haemorrhage
- •2.6. Are under 16 years of age
- •2.7. Have a known contra-indication to oxytocin therapy as listed in the Summary of marketing Product Characteristics
研究者
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