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Trials / Unknown

UnknownNCT04780412

Efficacy of Misoprostol in Prevention of Neonatal Respiratory Morbidity in Parturient at Early Term Elective Caesarian Section

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
210 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

Neonatal respiratory morbidities represent a common group of post natal complications including respiratory distress syndrome, transient tachypnea of newborn, and persistent pulmonary hypertension of newborn. It is thought that preoperative vaginal misoprostol administration may decrease the incidence of neonatal respiratory morbidity especially transient tachypnea of newborn. And therefore, it may decrease the incidence of admission to neonatal intensive care units for respiratory causes.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostolVaginal Misoprostol tablets in a dose of 50 microgram given 90-120 minutes before an elective caesarian section.
DRUGPlaceboVaginal placebo pills given 90-120 minutes before an elective caesarian section.

Timeline

Start date
2020-09-01
Primary completion
2021-03-01
Completion
2021-03-01
First posted
2021-03-03
Last updated
2021-03-03

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04780412. Inclusion in this directory is not an endorsement.

Efficacy of Misoprostol in Prevention of Neonatal Respiratory Morbidity in Parturient at Early Term Elective Caesarian S (NCT04780412) · Clinical Trials Directory