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The Impact of Maternal Obesity on Pregnancy Outcomes in El-Minia Locality

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02719873
Enrollment
330
Registered
2016-03-25
Start date
2016-08-31
Completion date
2017-07-14
Last updated
2017-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity During Pregnancy in Clinical Practice

Keywords

obesity , pregnancy , maternal and fetal outcome

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.

Interventions

OTHERThe impact of maternal obesity on pregnancy outcomes

observation of maternal obesity effect in foetal and maternal outcome

Sponsors

Minia University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* obese * pregnant * 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 \-

Design outcomes

Primary

MeasureTime frameDescription
Mode of deliveryonset of labor till endvaginal or Cesarean section
shoulder dystocia1 minute after delivery of the headarrest of shoulder more than one minute after delivery of the head
foetal macrosomiaat time of labour or elective CSfoetal weight at time of delivery more than 90th percentil

Secondary

MeasureTime frameDescription
postpartum hemorrhageonset of labor and for 6 weeks afterprimary or secondary blood loss through birth canal more than 500cc
postpatum maternal infectionend of labor and for 6weeks afterpostpartum signs of sepsis
neonatal ICU admissionone month after deliveryneonatal ICU admission

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026