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临床试验/EUCTR2010-020780-21-SE
EUCTR2010-020780-21-SE进行中(未招募)不适用

Paracervical block (PCB) during II-trimester abortion – a randomized controlled trial - Paracervical block (PCB) during II-trimester abortion – a randomized controlled trial

Department of Obstetrics and Gynaecology, Karolinska Institutet, Stockholm0 个研究点目标入组 125 人开始时间: 2011年2月22日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
125

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 according to ultrasound dating of pregnancy are pregnant in 13 weeks or more and wish to have an induced abortion at Söder Hospital will be asked if they want to participate in the study. Women must be 18 years or older and able to communicate in Swedish. The woman will receive oral and written information about the study and provide signed consent for their participation.
  • 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

  • Allergy to local anesthetics.

研究者

发起方
Department of Obstetrics and Gynaecology, Karolinska Institutet, Stockholm

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