Clinical Trials Directory

Trials / Completed

CompletedNCT01772381

Dexamethasone in Prevention of Respiratory Morbidity in Elective Caesarean Section in Term Fetus

Dexamethasone in Prevention of Respiratory Morbidity in Elective Caesarean

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
600 (actual)
Sponsor
Ain Shams Maternity Hospital · Academic / Other
Sex
Female
Age
22 Years – 44 Years
Healthy volunteers
Accepted

Summary

Introduction: Babies born at term by elective caesarean section (CS) and before onset of labor are more likely to develop respiratory complications than babies born vaginally. In developing countries resources are scarce and it is difficult to provide expensive treatments as neonatal care. Aim of the Work: To assess the effect of prophylactic dexamethasone administration before elective cesarean section at term in reducing neonatal respiratory complications. Patients and methods: 600 women were included in the study and were planned to have elective caesarean section. 300 received dexamethasone 12 mg twice, 12 hours apart 48 hours before delivery. 300 patients were the control group. The outcomes were: incidence of admission to neonatal intensive care unit (NICU), incidence of transient tachypnea of newborn (TTN), the incidence of respiratory distress syndrome (RDS) and the need for mechanical ventilation.

Detailed description

Dexamethasone which is a long acting corticosteroid can be used prior to elective cesarean section to decrease neonatal respiratory morbidity by enhacing fetal lung maturity.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneLong acting corticosteroid

Timeline

Start date
2010-03-01
Primary completion
2011-03-01
Completion
2011-06-01
First posted
2013-01-21
Last updated
2013-01-21

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT01772381. Inclusion in this directory is not an endorsement.