drugset / Trial / NCT07576881

Impact of Standardization on Outcomes Following Cervical Ripening

NCT07576881

Phase 2/3 Not yet recruiting 1158 enrolled Indiana University Indiana University Health · collab
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

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified

Indications