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
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