drugset / Trial / NCT07576881
Impact of Standardization on Outcomes Following Cervical Ripening
RandomizedParallel-groupOpen-labelTreatment
Summary
The primary purpose of this study is to determine if vaginal delivery rate is impacted by the use of standardized methods of cervical ripening. Additional outcomes will be evaluated including maternal and fetal outcomes of labor.
Timeline
- Start
- 2026-06
- Primary completion
- 2027-12
- Completion
- 2028-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Misoprostol | Other / unclassified | — | — |