跳至主要内容
临床试验/NCT01979835
NCT01979835已完成不适用

GYNEFIX-VIZ*: A STUDY OF SEROSAL-ANCHOR (SA) DISTANCE IN WOMEN IMMEDIATELY AND 6-8 WEEKS FOLLOWING INSERTION

Wiebe, Ellen, M.D.2 个研究点 分布在 1 个国家目标入组 1,030 人开始时间: 2013年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,030
试验地点
2
主要终点
Serosal-anchor Measurement

研究概览

简要总结

The GyneFix-Viz is a frameless copper intrauterine device (IUD) used for contraception. The GyneFix IUD has been marketed in Europe and Asia for about 10 years. The new anchor in the GyneFix IUD was designed to be more visible on ultrasound and this could improve safety by reducing failed insertions and perforations. We now need to know how easy it is for doctors to see and measure the distance of the anchor to the outside of the uterus. The purpose of this open, prospective, observational study is to assess the feasibility of measuring the distance from the serosa of the uterus to the anchor following insertion of the GyneFix-Viz and at follow-up 6-8 weeks later. Secondary objectives are to assess the ease and pain of insertion, the acceptability of the device to Canadian women and any complications. We will also compare expulsion rates in post-abortion and other women.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
16 Years 至 50 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • healthy women requesting intrauterine contraception
  • willing to have a GyneFix IUD for pregnancy prevention
  • able to return for a follow-up ultrasound
  • able to read and understand consent form

排除标准

  • Any contraindications precluding insertion of an IUD (e.g., infection, cancer of the uterus, malformation etc.)
  • Immediately after a pregnancy interruption > 10 weeks gestation

结局指标

主要结局

Serosal-anchor Measurement

时间窗: 6-8 weeks

endovaginal ultrasound measurement of the distance from the anchor of the device and the serosal surface of the uterus

次要结局

  • Complications(5 years)

研究者

发起方
Wiebe, Ellen, M.D.
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验