跳至主要内容
临床试验/EUCTR2016-000889-35-BE
EUCTR2016-000889-35-BE进行中(未招募)1 期

Comparison of two methods of administration of the epidural, by programmed intermittent bolus or continuous perfusion, on the incidence of instrumented deliveries and cesareans in primiparous women.

Centre Hospitalier Universitaire Brugmann0 个研究点目标入组 784 人开始时间: 2016年4月25日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
784

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

  • - Women over 18 years of age
  • - Primiparous
  • - Pregnancy over 36 weeks of gestational age and <42 weeks of gestational age
  • - Written informed consent
  • - Cervical dilatation between 3 and 6 cm at recruitment
  • - Single pregnancy
  • - Foetus in cephalic position
  • 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 784
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Participation refusal or epidural contra-indication
  • - Multiparous
  • - Allergy to the products used
  • - Twin pregnancy
  • - Height <1m55 and/or narrow pelvis, as shown by imagery
  • - Langage barrier
  • - Patients with a BMI superior or equal to 35 (computed with the weight at the beginning of the pregnancy)
  • - Cervical dilatation at recruitment <3 or >6 cm
  • - ASA 3 or 4
  • - Foetus in transverse or seat position

研究者

发起方
Centre Hospitalier Universitaire Brugmann

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