跳至主要内容
临床试验/NCT03668184
NCT03668184已完成不适用

What Are the Predictive Factors for Preeclampsia in Oocyte Recipients? - PREROVE

Rennes University Hospital2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2018年1月2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
150
试验地点
2
主要终点
occurrence of pre-eclampsia

研究概览

简要总结

The main goal is to determine which risk factors develop preeclampsia in this specific group of oocyte recipients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • All major patients with a pregnancy of more than 22 weeks of amenorrhea resulting from an oocyte donation in one of the study centers, having given birth between January 2010 and April 2017 and not opposed to participation in the study.

排除标准

  • all pregnancies resulting from an oocyte donation abroad, persons of legal age subject to legal protection (safeguard of justice, guardianship, tutorship) and persons deprived of their liberty.

结局指标

主要结局

occurrence of pre-eclampsia

时间窗: through study completion, an average of 1 year

次要结局

未报告次要终点

研究者

发起方
Rennes University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验