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临床试验/ISRCTN13763635
ISRCTN13763635招募中未知

Preconceptional transvaginal cervicoisthmic cerclage versus transvaginal cervicoisthmic cerclage in pregnancy for the prevention of preterm delivery in women with cervical insufficiency: a randomized controlled study

Health Bureau of Zhejiang Province0 个研究点目标入组 200 人开始时间: 2015年1月14日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
200

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

性别
Female

入选标准

  • Current inclusion criteria as of 04/03/2019:
  • 1. A history of at least 1 previous late inevitable abortion or spontaneous preterm delivery
  • 2. Previous conization of the cervix or cervical laceration by assisted vaginal delivery, and the residual cervix is less than 25mm
  • 3. All patients should be >=18 years and younger than 35 years old
  • 4. All patients are able to conceive
  • Previous inclusion criteria:
  • 1. A history of at least 2 previous late inevitable abortion or spontaneous preterm delivery
  • 2. Previous conization of the cervix or cervical laceration by assisted vaginal delivery, and the residual cervix is less than 25mm
  • 3. All patients should be >=18 years and younger than 35 years old
  • 4. All patients are able to conceive

排除标准

  • 1. Older than 35 years old
  • 2. Patients with a successful or failed cerclage applied in a previous pregnancy
  • 3. Patients with congenital uterine dysplasia: Mediastinum uterus, bicornuate uterus, rudimentary horn of uterus, et al.
  • 4. Patients with protein C, protein S, or antithrombin III de?ciency
  • 5. Patients who are pregnant

研究者

发起方
Health Bureau of Zhejiang Province

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