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Clinical Trial Summary

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.


Clinical Trial Description

- 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02788305
Study type Observational
Source Kasr El Aini Hospital
Contact
Status Completed
Phase N/A
Start date May 1, 2016
Completion date June 30, 2017

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