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Clinical Trials/NCT02719873
NCT02719873
Completed
Not Applicable

The Impact of Maternal Obesity on Pregnancy Outcomes in El-Minia Locality a Case Control Survey Study

Minia University1 site in 1 country330 target enrollmentAugust 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity During Pregnancy in Clinical Practice
Sponsor
Minia University
Enrollment
330
Locations
1
Primary Endpoint
Mode of delivery
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

A study will carried out over a period of one year , all obese pregnant women as diagnosed with BMI at the time of 1st ANC visit and before labor ,observation of events during both intra-partum &postpartum periods it will be recorded.outcome will compared with normal other pregnant women

Detailed Description

It is known that obesity during pregnancy has drawbacks for both maternal and foetal outcome The aim of this study is to evaluate and measure the proportion of the adverse pregnancy outcomes attributable to maternal obesity and so reaching to recommendations in order to improve the outcomes and wellbeing of these women and their children.patient will be divided into two groups control group with normal BMI and study group and both compared as regard foetal and maternal outcome The assessed fetal variables will be: fetal birthweight \& incubators admission. Data will be retrieved from patients before labor and from investigator observation both intrapartum and postpartum.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
July 14, 2017
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Minia University
Responsible Party
Principal Investigator
Principal Investigator

Reham Elkhateeb

doctor

Minia University

Eligibility Criteria

Inclusion Criteria

  • age 18 -40
  • single viable cephalic foetus

Exclusion Criteria

  • less than 18 years more than 40 years associated medical disorders patient refusal non cephalic presentation

Outcomes

Primary Outcomes

Mode of delivery

Time Frame: onset of labor till end

vaginal or Cesarean section

foetal macrosomia

Time Frame: at time of labour or elective CS

foetal weight at time of delivery more than 90th percentil

shoulder dystocia

Time Frame: 1 minute after delivery of the head

arrest of shoulder more than one minute after delivery of the head

Secondary Outcomes

  • neonatal ICU admission(one month after delivery)
  • postpartum hemorrhage(onset of labor and for 6 weeks after)
  • postpatum maternal infection(end of labor and for 6weeks after)

Study Sites (1)

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