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Misoprostol Before Elective Caesarean Section for Decreasing the Neonatal Respiratory Morbidity

Cesarean Delivery Affecting Fetus Clinical Trial

Official title:
Misoprostol Before Elective Caesarean Section for Decreasing the Neonatal Respiratory Morbidity: A Randomized Controlled Trial

Clinical Trial Summary

Neonatal respiratory distress may occur in either term or preterm newborns with a higher relative risk in preterm, and whether born vaginally or through caesarean section, but in a higher percentage after elective caesarean section whose rate is rising.

Prostaglandins may be given about one hour before an elective caesarean section after excluding the presence of contraindication to their use to decrease the neonatal respiratory diseases and thus, the number of children who suffered from bronchopulmonary dysplasia that occurs frequently in children who had previously TTN will diminish.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03031353
Study type Interventional
Source Ain Shams University
Contact Ahmed M kotb, MD
Phone 01008681999
Email ahmedmkotp@hotmail.com
Status Recruiting
Phase N/A
Start date January 2017
Completion date June 2018
View Details
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