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临床试验/NCT03095014
NCT03095014已完成1 期

Cesarean Myomectomy : Safety and Risk of Intrauterine Synechiae

Zagazig University0 个研究点目标入组 76 人开始时间: 2010年1月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
76
主要终点
Mean change in Haemoglobin in gm/dl

研究概览

简要总结

Cesarean Myomectomy, safety and effect on uterine cavity.

详细描述

this study aims to compare between women who underwent Cesarean Myomectomy and those who underwent Cesarean section only regarding the procedure safety and whether uterine cavity was affected later on.

研究设计

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

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •full term
  • •had uterine myoma

排除标准

  • •history of coagulation disorder
  • •antepartum hemorrhage
  • •previous myomectomy
  • •where additional operative procedures were performed

研究组 & 干预措施

Cesarean Myomectomy

Experimental

Myomectomy plus Cesarean section

干预措施: Cesarean Myomectomy (Procedure)

Cesarean section

Active Comparator

Cesarean section only

干预措施: Cesarean section (Procedure)

结局指标

主要结局

Mean change in Haemoglobin in gm/dl

时间窗: 24 hours

pre-operative Haemoglobin minus post-operative Haemoglobin level

次要结局

  • Duration of operation in hours(2 hours)
  • intrauterine adesion adhesions(3 months)

研究者

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

IBRAHIM ABD ELGAFOR

assistant professor

Zagazig University

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