Misoprostol Before Caesarean Section
Condition(s) studied
Investigational drug(s) / intervention(s)
Misoprostol: administration of 100mg of misoprostol to evaluate the efficacy of Misoprostol before elective cesarean section in pregnant women with gestational age less than 38 weeks for preventing the occurrence of neonatal respiratory morbidity.
Study summary
The aim of our study is to evaluate the efficacy of Misoprostol before elective cesarean section in pregnant women with gestational age less than 38 weeks for preventing the occurrence of neonatal respiratory morbidity.
Eligibility
Primary outcome measure(s)
- the incidence of Transient tachypnea of the newborn which defined by increase respiratory rate more than 60 cycle per minute in pregnant women with gestational age less than 38 weeks before elective cesarean section — in the first 5 minute after delivery of fetus post operative
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Kafr El-sheikh University Hospital | Kafr Ash Shaykh, Egypt | Egypt | Recruiting |
More Kafrelsheikh University trials in Egypt
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06946914 on ClinicalTrials.gov ↗ ← All trials in Egypt