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

Dexamethasone in Prevention of Respiratory Morbidity in Elective Caesarean

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01772381
Enrollment
600
Registered
2013-01-21
Start date
2010-03-31
Completion date
2011-06-30
Last updated
2013-01-21

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

Conditions

Transient Tachypnea of the Newborn

Keywords

Dexamethasone, term, elective cesarean section

Brief 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.

Interventions

DRUGDexamethasone

Long acting corticosteroid

Sponsors

Ain Shams Maternity Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
22 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

* Previous caesarean section * Complete 37 week calculated from the first day of the last menstrual period.

Exclusion criteria

* Obstetric complications such as pre-eclampsia, antepartum hemorrhage or known fetal anomaly. * Hypertensive patients. * Chronic disease e.g. diabetes mellitus. * Known renal disease. * Pre-operative infection.

Design outcomes

Primary

MeasureTime frameDescription
Special care baby unit24 hoursSpecial care baby unit admission for babies with respiratory distress

Secondary

MeasureTime frameDescription
Severity of respiratory distress24 hoursSeverity of respiratory distress and the level of care in response

Countries

Egypt

Outcome results

None listed

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