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Comparison Between Amniotic Fluid Lamellar Body Count and Fetal Pulmonary Artery Doppler Indices in Predicting Fetal Lung Maturity

Phase 3
Conditions
Preterm Labour
Interventions
Device: Amniotic fluid lamellar body count
Device: Fetal pulmonary artery Doppler
Registration Number
NCT02331199
Lead Sponsor
Cairo University
Brief Summary

The investigators will study 200 women with singleton pregnancies presented with prelabor preterm rupture of membranes or undergoing cesarean section (CS). Amniotic fluid lamellar body count (LBC) and fetal pulmonary artery Doppler will be done to all women. LBC and fetal pulmonary artery Doppler will be correlated with fetal outcome

Detailed Description

Neonatal respiratory distress syndrome (RDS) remains a major cause of neonatal morbidity and mortality. A recent epidemiologic study in the United States estimates that there are 80,000 cases of neonatal RDS each year, resulting in 8500 deaths and hospital costs in excess of $4.4 billion.

A number of biochemical tests have been developed to predict the risk of RDS and assist obstetric care providers in delivery timing. Amniotic fluid lamellar body count (LBC) is an important biophysical test, based on measuring the concentration of pulmonary surfactant in amniotic fluid. It can be effectively used to assess fetal lung maturity. A noninvasive test for fetal lung maturity (FLM) would be useful to minimize the need for invasive testing and would be more acceptable to women. Fetal pulmonary artery Doppler waveform acceleration/ejection time may provide a noninvasive means of determining fetal lung maturity with relatively acceptable levels of sensitivity, specificity, and predictive values.

The investigators will study 200 women with singleton pregnancies presented with prelabor preterm rupture of membranes or undergoing cesarean section (CS). Amniotic fluid lamellar body count (LBC) and fetal pulmonary artery Doppler will be done to all women. LBC and fetal pulmonary artery Doppler will be correlated with fetal outcome.

Quantitative data will be statistically represented in terms of mean ± standard deviation (± SD) while categorical data will be represented as frequency and percentage. Comparison of quantitative data will be done using Mann Whitney U test for independent samples while categorical data will compared using Chi squared test or Fisher exact test when appropriate. A probability value (p value) less than 0.05 will be considered significant.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
200
Inclusion Criteria
  • Singleton pregnancies without any major congenital anomalies.
  • Gestation between 32-36 weeks
  • Women presenting preterm pre-labour ruptured membranes or undergoing a cesarean section.
Exclusion Criteria
  • Patients with major fetal anomalies.
  • Bloody or meconium stained amniotic fluid
  • preexisting maternal medical conditions (eg, diabetes, renal disease, hypertensive disorders, vaginal bleeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
preterm labourAmniotic fluid lamellar body count200 women with preterm prelabour ruptured membranes or undergoing preterm CS
preterm labourFetal pulmonary artery Doppler200 women with preterm prelabour ruptured membranes or undergoing preterm CS
Primary Outcome Measures
NameTimeMethod
Respiratory distress syndrome (RDS)1 day after delivery

RDS will be diagnosed clinically by the presence of tachypnea, working respiratory muscles, expiratory grunt, and chest x-ray.

Secondary Outcome Measures
NameTimeMethod
Need for incubation1 day after delivery

It will be recorded if the pediatrician decides to incubate the neonate. The reason for incubation e.g. ventilation, hypoxia, ischemia will be recorded.

Trial Locations

Locations (2)

Al Galaa maternity fospital

🇪🇬

Cairo, Egypt

Cairo university hospitals

🇪🇬

Cairo, Egypt

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