ISRCTN89932581已完成不适用
A double-blind randomised trial of 250 µg versus 500 µg bolus dose of terbutaline as a tocolytic agent in external cephalic version
niversity of Malaya Medical Centre (Malaysia)0 个研究点目标入组 104 人开始时间: 2009年5月13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
- 104
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. Non-cephalic presentation
- •2. Singleton pregnancy
- •3. Gestation greater than or equal to 36 weeks (check for early confirmation of gestational age)
- •4. Intact membranes
- •5. Reassuring foetal status on cardiotocograph
排除标准
- •1. Known gross foetal anomaly
- •2. Severe hypertension (greater than or equal to 160/110 mmHg or confirmed pre-eclampsia)
- •3. Growth restricted foetus (estimated foetal weight less than 2 kg or ultrasound-derived foetal abdominal circumference less than 10 centile on our chart)
- •4. Oligohydramnios (amniotic fluid index [AFI] less than 5)
- •5. Antepartum haemorrhage within last 7 days
- •6. Uterine scar from any source
- •7. Known allergy to terbutaline
- •8. Other potential obstetric indication for caesarean delivery:
- •8.1. Placenta praevia
- •8.2. Suspected macrosomia greater than 4 kg
- •8.3. Uterine anomaly (small fibroids not causing obstruction are acceptable)
- •8.4. Obstructive pelvic tumour
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