Clinical Trials Directory

Trials / Unknown

UnknownNCT03031353

Misoprostol Before Elective Caesarean Section for Decreasing the Neonatal Respiratory Morbidity

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
170 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostolMisoprostol is given before elective cesarean section as prophylaxis against post partum hemorrhage
DRUGPlacebosplacebos tablet will be given before elective Cesarean sections

Timeline

Start date
2017-01-01
Primary completion
2018-05-01
Completion
2018-06-01
First posted
2017-01-25
Last updated
2018-05-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03031353. Inclusion in this directory is not an endorsement.