Hémorragies et Maladie Veineuse Thromboembolique du Post-partum : Epidémiologie, Etudes Des déterminants Cliniques et Biologiques
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20,241
- 试验地点
- 6
- 主要终点
- Postpartum Hemorrhage
研究概览
简要总结
The aim of this study is to evaluate the frequencey and the determinants of postpartum major complications (hemorrhage and thrombosis) up to 3 months after delivery in the maternity hospitals of Finistère (Bretagne - France)
详细描述
This is an analytical observational prospective multicenter cohort study , conducted on all the maternity hospitals in Finistère (Bretagne - France), with a biological collection.
This protocol allows to study all women at risk of PPH (Postpartum Hemorrhage) and postpartum venous thromboembolic disease, including maternity level 1-3 without case selection. The prospective nature of the study should provide a more detailed analysis of exposures in this particular population of women (risk factors related to the field, childbirth, the postpartum events ...).
The events of interest were PPH and venous thromboembolic disease.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 16 Years 至 —（Child, Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Any woman giving birth and supported in one of Gynaecology Obstetrics services of a maternity Finistere.
- •Women ≥ 16 at the time of the collection of non-opposition.
- •For minor patients: understanding the patient and at least one parent.
- •All births ≥ 15 weeks gestation.
排除标准
- •Home Birth
- •Expressed opposition to participation in this study.
- •Childbirth under X.
- •Parent (s) uninformed of the pregnancy of their child.
结局指标
主要结局
Postpartum Hemorrhage
时间窗: 2 days
Volume of blood loss up to 48 hours after delivery and / or weight compresses collected at delivery, and / or diagnosis of the clinician
Symptomatic thromboembolic events
时间窗: 3 month
次要结局
未报告次要终点