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临床试验/NCT03824873
NCT03824873已完成3 期

Internal Iliac Artery Ligation Before Cesarean Hysterectomy in Morbidly Adherent Placenta: A Randomized Clinical Trial

Ain Shams University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年3月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
40
试验地点
1
主要终点
Amount of blood loss

研究概览

简要总结

40 pregnant females at term diagnosed with morbidly adherent placenta and planned for elective cesarean section were recruited and randomized to 2 groups. Group A: Internal iliac ligation followed by cesarean hysterectomy. Group B: cesarean hysterectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
25 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Placenta previa accreta
  • •Previous 2 cesarean section
  • •completed her family
  • •Hemoglobin > 11 gm/dl
  • •Elective cesarean hysterectomy

排除标准

  • •Anemia ( Hemoglobin < 11 gm/dl)
  • •Not completed her family
  • •BMI > 35 Kg/m2
  • •Bleeding tendency
  • •Emergengy cesarean section
  • •Thrombophilia

研究组 & 干预措施

internal iliac artery ligation + cesarean hysterectomy

Active Comparator

干预措施: Internal iliac artery ligation (Procedure)

internal iliac artery ligation + cesarean hysterectomy

Active Comparator

干预措施: cesarean hysterectomy (Procedure)

cesarean hysterectomy

Active Comparator

干预措施: cesarean hysterectomy (Procedure)

结局指标

主要结局

Amount of blood loss

时间窗: intraoperative

Amount of Blood transfusion needed in mililiters

时间窗: 24 hours

次要结局

  • change of hematocrit(24 hours)
  • change of hemoglobin(24 hours)
  • operative time(intraoperative)
  • incidence of injury of important structures during operation(intraoperative)

研究者

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

Mohamed S Sweed, MD

Principal Investigator

Ain Shams University

研究点 (1)

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