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临床试验/NCT00890474
NCT00890474已完成3 期

Moxibustion for Fetus in Breech Presentation

University Hospital, Geneva1 个研究点 分布在 1 个国家目标入组 212 人开始时间: 2004年10月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
212
试验地点
1
主要终点
Cephalic presentation at delivery or before external cephalic version

研究概览

简要总结

Objective: To evaluate moxibustion of the BL67 acupoint between 34 and 38 weeks of gestation to facilitate cephalic version of breech presentation in a Western setting. The hypothesis is that moxibustion increase the likelihood of cephalic version.

Design: Randomised controlled trial Setting: University hospital. Population: A total of 212 consenting women between 34 and 36 weeks of gestation with a single fetus in breech presentation will be randomised to moxibustion (n=106) or expectant management (n=106).

Main Outcome Measure: Cephalic presentation at delivery or before external cephalic version.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Care Provider)

入排标准

性别
Female
接受健康志愿者

入选标准

  • Breech presentation
  • 34 to 36 weeks of gestation
  • Single fetus

排除标准

  • Uterine malformation
  • Placenta praevia
  • Transverse lie

结局指标

主要结局

Cephalic presentation at delivery or before external cephalic version

时间窗: end of pregnancy

次要结局

  • Mode of delivery(end of pregnancy)
  • Women's views on the intervention(end of pregnancy)
  • External cephalic version(end of pregnancy)

研究者

申办方类型
Other

研究点 (1)

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