跳至主要内容
临床试验/ISRCTN89932581
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

研究者

发起方
niversity of Malaya Medical Centre (Malaysia)

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