跳至主要内容
临床试验/EUCTR2013-001775-20-SE
EUCTR2013-001775-20-SE进行中(未招募)1 期

A phase 2 study investigating the feasibility of using a topical formulation of lidocaine (SHACT) for hysteroscopy in women.

Pharmanest AB0 个研究点目标入组 10 人开始时间: 2013年5月7日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
10

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

  • Patients planned for hysteroscopy under anaesthesia at Kvinnokliniken, Södersjukhuset
  • Has given written informed consent after verbal and written information
  • 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 10
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1

排除标准

  • Contraindication for hysteroscopy with lidocaine instillation at the discretion of the principal investigator
  • Known allergy to lidocaine
  • Recidivating porphyria

研究者

发起方
Pharmanest AB

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