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Clinical Trials/NCT02788305
NCT02788305
Completed
Not Applicable

Effect of Maternal Obesity on Labour Induction in Postdate Pregnancy

Kasr El Aini Hospital1 site in 1 country288 target enrollmentMay 1, 2016

Overview

Phase
Not Applicable
Intervention
Misoprostol
Conditions
Obesity
Sponsor
Kasr El Aini Hospital
Enrollment
288
Locations
1
Primary Endpoint
route of delivery vaginal or caesarean section.
Status
Completed
Last Updated
8 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
May 1, 2016
End Date
June 30, 2017
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Kasr El Aini Hospital
Responsible Party
Principal Investigator
Principal Investigator

heba mahmoud ibrahim marie

lecturer at kaselaini hospitals

Kasr El Aini Hospital

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • 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).

Arms & Interventions

non obese

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

Intervention: Misoprostol

obese

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

Intervention: Misoprostol

Outcomes

Primary Outcomes

route of delivery vaginal or caesarean section.

Time Frame: 48 hours from the start of induction

Partogram is used to access the progress of labour

Secondary Outcomes

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

Study Sites (1)

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