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临床试验/NCT02788305
NCT02788305已完成不适用

Effect of Maternal Obesity on Labour Induction in Postdate Pregnancy

Kasr El Aini Hospital1 个研究点 分布在 1 个国家目标入组 288 人开始时间: 2016年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
288
试验地点
1
主要终点
route of delivery vaginal or caesarean section.

研究概览

简要总结

This study investigate the progression of labour in 144 normal weight pregnant women (BMI <30) and 144 obese pregnant women (BMI >30) , not in labor admitted for induction of labor. These women are to be investigated for success of induction of labor.

详细描述

  • This prospective study will be conducted for 144 obese and 144 non obese ), post date (>41 wks), not in labor.

  • Woman is classified as obese if BMI >=30.

  • Prolonged pregnancy was defined as delivery on or after (41+0 weeks) of gestation.

  • First informed consent will be obtained.

  • Determination of gestational age

  • Proper history taking, general and abdominal examinations will be done then digital examination will be performed to determine bishop score.

  • And obstetric U/S scan will be done and by which the following data will be obtained :

  • Fetal biometry

  • Fetal heart activity

  • Presentation

  • Localization of the placenta.

  • Amount of amniotic fluid.

  • Exclude multifetal pregnancy.

  • Induction of labor will be done using vaginal misoprostol according to the estimated Bishop score.

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
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant woman.
  • Post date >= 41 weeks.
  • Absent onset of labor.
  • Patient acceptance to join the study after signing an informed consent.

排除标准

  • Placenta previa and or vasa previa.
  • Previous caesarean section(CS).
  • Multiple gestation
  • Any patient who will refuse to be a part of the study.
  • Intra- uterine fetal death (IUFD).

研究组 & 干预措施

non obese

BMI<30. Misoprostol is given for induction of labour according to Bishop score

干预措施: Misoprostol (Drug)

obese

BMI>30. Misoprostol is given for induction of labour according to Bishop score

干预措施: Misoprostol (Drug)

结局指标

主要结局

route of delivery vaginal or caesarean section.

时间窗: 48 hours from the start of induction

Partogram is used to access the progress of labour

次要结局

  • maternal haemorrhage(48 hours from the start of induction)

研究者

发起方
Kasr El Aini Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

heba mahmoud ibrahim marie

lecturer at kaselaini hospitals

Kasr El Aini Hospital

研究点 (1)

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