跳至主要内容
临床试验/NL-OMON40263
NL-OMON40263已完成不适用

RCT comparing insertion of levonorgestrel releasing intrauterine system (Mirena) during the menstruation compared with random insertion beyond menstruations in patient-perceived pain. - Timing Insertion MirEna trial (TIME trial)

Maxima Medisch Centrum0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Women who menstruate with a wish for LNG-IUS

排除标准

  • * Women with an abnormal uterine cavity (myomas, polyps) determined by a TransVaginalUltrasound (TVU)
  • * Women with a failed insertion in a previous attempt, or with a LNG-IUS in situ and wish for change
  • * Women younger than 18 years
  • * Peri- or postmenopausal women
  • * Women with a positive pregnancy test or who had unprotected intercourse since their menses
  • * Amenorrhea after pregnancy

研究者

发起方
Maxima Medisch Centrum

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