Effect of Single Dose Antenatal Betamethasone on Neonatal Respiratory Morbidity After Elective Cesarean
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- STATUS
- Recruiting
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- participants needed
- 400
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- sponsor
- Makassed General Hospital
Summary
Patients undergoing elective C-section will be randomized into two groups. The first group will receive one dose of Betamethasone at least 24 hours before scheduled C-section. The second group will receive placebo.
Description
This is a prospective double blinded randomized clinical trial. Patients will be randomized into two groups. Group A will receive one dose of Betamethasone at least 24 hours before scheduled C-section. Group B will receive placebo. The maternal and neonatal outcomes will be studied in order to assess the effect of Betamethasone on respiratory morbidity of the newborn infant.
Details
| Condition | Respiratory Morbidity |
|---|---|
| Age | 17-45 years |
| Treatment | Placebo, Betamethasone |
| Clinical Study Identifier | NCT04407975 |
| Sponsor | Makassed General Hospital |
| Last Modified on | 19 February 2024 |
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