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Effect of Maternal Body Mass Index on Labor Progress in Nulliparous Women

Revising the Norms of Labor Progress in Egyptian Nulliparous Women in Relation to Maternal Body Mass Index Categories

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02686073
Enrollment
600
Registered
2016-02-19
Start date
2016-02-20
Completion date
2017-02-28
Last updated
2017-07-12

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

Conditions

Labor Progress

Keywords

BMI, progress of labor, nulliparous women

Brief summary

Study the rate of progress of labor among nulliparous women belonging to different body mass index groups, & observe how does this variation in maternal body mass index may affect the course of labor.

Detailed description

For nulliparous cases presenting to the labor ward, maternal height & weight will be collected at the time of admission to calculate the BMI (body mass index) & further classified according to WHO (World Health Organization) categories. Putting into consideration the physiological increase in BMI related to pregnancy, the overweight participants whose BMI (25-29.9) will be combined with the normal range BMI (18.5-24.9) category. Labor characteristics of these participants will be then compared with those of the underweight (BMI less than 18.5) & obese (BMI 30 or higher) participants.Females are assigned in one of 3 groups based on their BMI; Underweight group (BMI \<18.5kg/m2), Control group whose BMI within normal range (18.5-29.9 kg/m2),& Obese group (BMI more than or equal 30kg/m2). Labor management protocols are fixed. Data on labor progression are collected, including cervical dilatation, cervical effacement, head station & descent. The median duration of labor , estimated by rate of cervical dilatation in cm, will be used as a measurement of labor progression in each group. A cesarean section for abnormal labor pattern will be documented as failure of progress.

Interventions

None listed

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* nulliparous women in active phase of labor, with an age range from 20 to 40 years. Full term pregnancy, singleton, viable fetus, cephalic (vertex) presentation, occipito-anterior position.

Exclusion criteria

* Multiparous women. Preterm labor. Passed date delivery. Multiple gestation. Large fetal weight (more than 4000g). Intrauterine fetal death. Intrauterine fetal growth restriction. Major fetal congenital anomalies. Rupture of membranes before onset of active labor. Fetal malposition or malpresentation. Inadequate pelvis or cephalopelvic disproportion. Maternal medical disorder. Induction of labor by oxytocin or prostaglandins. Conditions requiring urgent delivery eg antepartum haemorrhage, fetal distress, cord prolapse.

Design outcomes

Primary

MeasureTime frameDescription
rate of cervical dilatationevery 2 hours during active phase of labor, from admission to the labor ward until second stage of labor.in centimeters

Secondary

MeasureTime frameDescription
descent of fetal headevery 2 hours during active phase of labor, from admission to the labor ward until second stage of laborhead station

Other

MeasureTime frameDescription
duration of active phase of laborall through the course of labor, individually assessed for each participant, starting from the time of admission to labor ward until start of second stage of labortotal duration in hours
duration of second stage of laborfrom start of second stage of labor ( full cervical dilatation) until delivery of fetustotal duration in minutes
mode of deliverylaborvaginal delivery or cesarean section

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026