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Impact of Standardization on Outcomes Following Cervical Ripening

StatusNot Yet Recruiting
PhasePhase 2/3
Started2026-06
View on ClinicalTrials.gov ↗
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.
Trial Details
NCT Number NCT07576881
Lead Sponsor Indiana University
Collaborators: Indiana University Health
Conditions Pregnancy
Enrollment 1,158 participants
Start Date 2026-06
Primary Completion 2027-12 (estimated)
Study Completion 2028-04 (estimated)
Updated on ClinicalTrials.gov 2026-05-08