ACTRN12609000985280已完成未知
A pilot randomised controlled trial (RCT) to determine the acceptability to randomization and to determine a sample size for an appropriately powered RCT to evaluate the effectiveness and cost effectiveness of moxibustion for cephalic version
niversity of Western Sydney0 个研究点目标入组 30 人开始时间: 2009年11月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Pregnant women, aged at least 18 years, a singleton breech presentation, normal
- •fetal biometry with a gestational age equal to or more than 34 weeks. An ultrasound scan will be required to confirm the type of breech presentation and the location of the placenta.
排除标准
- •Twin pregnancy, risk of premature birth, heart or kidney disease affecting the
- •mother, placenta previa, a history of antepartum hemorrhage, intrauterine growth restriction, hypertensive disease, isoimmunization, previous uterine operations, uterine anomaly, prelabor
- •rupture of the membranes, multiple pregnancy, fetal congenital abnormality, contraindication to vaginal delivery, or fetal death in utero.
研究者
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