ChiCTR1800014589进行中（未招募）不适用
使用 FloSeal 來停止胎盤床出血後的宮腔粘連的發生率
Nil1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 1990年1月1日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- To determine the incidence of intrauterine adhesion or Asherman’s syndrome after usage of Floseal to control postpartum haemorrhage
研究概览
简要总结
評估使用 FloSeal 來停止胎盤床出血後的宮腔粘連發生率的效果
研究设计
- 研究类型
- 观察性研究
- 主要目的
- 单臂
入排标准
- 性别
- Female
入选标准
- •All women presenting to our unit with use of FloSeal to control postpartum haemorrhage during Caesarean Section will be invited to join the study.
排除标准
- •Women who did not have Floseal applied in intrauterine cavity during Caesarean
研究组 & 干预措施
Case series
All women who had Floseal applied to intrauterine cavity during Caesarean section will be invited to participate in the study by our research assistant. For those who agree to join the study, an outpatient hysteroscopy will be performed within 3-6 months from their Caesarean section by a designated team
结局指标
主要结局
To determine the incidence of intrauterine adhesion or Asherman’s syndrome after usage of Floseal to control postpartum haemorrhage
时间窗: 3-6 months from their Caesarean section
次要结局
未报告次要终点
研究者
研究点 (1)
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