Clinical Trial

Impact of Standardization on Outcomes Following Cervical Ripening

Name: Impact of Standardization on Outcomes Following Cervical Ripening — clinical trial record (NCT07576881)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

Not Yet Recruiting Phase 2/3

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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.

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