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临床试验/EUCTR2009-012752-24-GB
EUCTR2009-012752-24-GB进行中(未招募)不适用

High or Low Dose Syntocinon (Oxytocin) for delay in labour - HOLDS

niversity of Birmingham0 个研究点开始时间: 2010年4月16日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

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

  • Inclusion criteria
  • Eligible women included
  • Consenting nulliparous women with a singleton pregnancy at term (37-42 weeks) gestation.
  • Confirmed delay in labour as defined by NICE Intrapartum Care Guideline and with ruptured membranes.
  • Labour is established when there are regular painful contractions and progressive cervical dilation from 4cm. Delay is suspected when cervical dilatation of <2cm in 4 hours occurs once labour is established. Delay is confirmed when progress of <1cm in 2 hours is found on repeat vaginal examination.
  • Are the trial subjects under 18? yes
  • 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

  • Exclusion criteria include
  • Under 16 years old
  • multiple pregnancy,
  • existing maternal or fetal disease or concern,
  • gestational diabetes
  • previous uterine surgery,
  • vaginal bleeding in this pregnancy of clinical significance or
  • contra-indication to oxytocin therapy

研究者

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