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
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | Misoprostol is given before elective cesarean section as prophylaxis against post partum hemorrhage |
| DRUG | Placebos | placebos 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.