跳至主要内容
临床试验/NCT02694341
NCT02694341撤回不适用

Bakri Ballon With or Without Abdominal Traction Stitch in Management of Uterine Bleeding in Cases of Placenta Previa

Assiut University2 个研究点 分布在 1 个国家开始时间: 2018年12月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Percentages of failure of Bakri Balloon either rupture of balloon or slippage of balloon.

研究概览

简要总结

The Bakri intrauterine balloon can achieve haemostasis in cases of postpartum haemorrhage, including haemorrhage associated with placenta previa by compressing the lower uterine segment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

性别
Female
接受健康志愿者

入选标准

  • All women delivered and presented with primary atonic PPH
  • Women who accepted to participate

排除标准

  • Traumatic PPH as excluded by examination under anesthesia.
  • With any suspected or clinical evidence of uterine infection
  • Women diagnosed to have preeclampsia or eclampsia after delivery.
  • Women who had DM during pregnancy
  • Women with history of DVT or other thromboembolic complication
  • Women with history of rheumatic heart disease.
  • Women with coagulation defects.

结局指标

主要结局

Percentages of failure of Bakri Balloon either rupture of balloon or slippage of balloon.

时间窗: 24 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmed Mohamed Abbas

Dr

Assiut University

研究点 (2)

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