Overview

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

Status:
Completed
Trial end date:
2011-06-01
Target enrollment:
0
Participant gender:
Female
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.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ain Shams Maternity Hospital
Treatments:
BB 1101
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Criteria
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.