ISRCTN14802064已完成不适用
Oral nifepidine versus subcutaneous terbutaline tocolysis for external cephalic version: A double blind randomised trial
niversity of Malaya Medical Centre (Malaysia)0 个研究点目标入组 90 人开始时间: 2008年7月31日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 90
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. Breech presentation or transverse lie
- •2. Viable, singleton pregnancy
- •3. Gestation age 36 to 41 weeks
- •4. Intact membranes
- •5. Not in established labour
排除标准
- •1. Known gross foetal anomaly
- •2. Severe hypertension
- •3. Intrauterine growth restriction
- •4. Oligohydramnios
- •5. Antepartum haemorrhage within last 3 months
- •6. Uterine scar from any source
- •7. Known allergy to nifedipine or terbutaline
- •8. Other potential obstetric indication for Caesarean delivery
- •8.1. Placenta praevia
- •8.2. Suspected macrosomia >4 kg
- •8.3. Uterine anomaly
- •8.4. Obstructive pelvic tumour
研究者
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