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
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | Vaginal Misoprostol tablets in a dose of 50 microgram given 90-120 minutes before an elective caesarian section. |
| DRUG | Placebo | Vaginal 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.