EUCTR2008-007344-34-NL进行中（未招募）不适用
External Cephalic Version with uterine relaxation: atosiban versus fenoterol, a multi-centre trial - ECV: atosiban vs fenoterol
Academic Medical Centre0 个研究点开始时间: 2009年5月25日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •1.Live singleton fetus
- •2.Breech presentation
- •3.Gestational age of 32 weeks and onwards
- •4.Maternal age of 18 years or more
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Maternal exclusion criteria;
- •-Any contra-indications to labour or vaginal birth (eg placenta praevia)
- •-Any contra-indication to ECV:
- •- A scarred uterus other than transverse in the lower segment
- •- Known uterine anomalies
- •- Placental abruption in the obstetric history
- •- Preeclampsia or eclampsia
- •- Third trimester blood loss
- •- Ruptured membranes
- •-Any contra-indication to atosiban or fenoterol:
- •- Cardiovascular disease
- •- Hyperthyreoidism
- •- Elevated liver enzymes or renal dysfunction
- •- Infection of the amniotic cavity
- •- Simultaneous use of prostaglandin inhibitors, beta-blockers (labetalol
- •(trandate)), xanthine derivatives (theofylline), tricyclic antidepressants,
- •calcium, vitamin D, mineralocorticoids.
- •- Use of prostaglandin inhibitors, beta-blockers (labetalol) tricyclic
- •antidepressants.
- •Fetal exclusion criteria;
- •-Suspected severe intrauterine growth restriction ( assessed by ultrasonography) or severe oligohydramnios (deepest pool <
- •-Fetal anomalies or an extended fetal head (very rare)
- •-Non reassuring signs of fetal well-being; non-reassuring fetal heart rate
研究者
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