跳至主要内容
临床试验/NL-OMON49341
NL-OMON49341已完成不适用

PREvention of intrauterine adhesion after hysteroscopic surgery with novel deGradable film - PREG1

WOMED0 个研究点目标入组 12 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
12

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 * 40 years AND no childbearing wish until the second look hysteroscopy,
  • OR history of permanent sterilization;
  • * Subject scheduled for myomectomy for one or more myoma(s) where one myoma is
  • at least 10mm in size (*10mm) as estimated by pre-operative ultrasound
  • measurement of the largest diameter
  • * Hysterometry prior to device insertion * 6cm and * 9cm.
  • * Subjects who are willing to provide a written informed consent as approved by
  • the applicable Ethics Committee prior to participating in this clinical
  • investigation.
  • * Subjects who can comply with the study follow-up or other study requirements

排除标准

  • * Current pregnancy
  • * Abnormal uterine cavity
  • * Known or suspected endometrial hyperplasia
  • * Medical history of cervical or endometrial cancer

研究者

发起方
WOMED

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