Clinical Trial

Ripening Approaches for Prompt Induction and Delivery - Sequential Versus Concurrent Dilapan-S and Misoprostol to Achieve Vaginal Delivery (RAPID-DS)

Study acronym: RAPID-DS
Not Yet Recruiting
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Summary
The purpose of this study is to compare the effectiveness of sequential versus combined multimodal cervical ripening strategies to achieve vaginal delivery within 24 hours among nulliparous patients with singleton, vertex pregnancies at term undergoing induction of labor.
Trial Details
NCT Number NCT07717502
Lead Sponsor Ochsner Health System
Collaborators: Medicem International
Conditions Nulliparous Women Who Scheduled for Labor Induction, Pregnancy
Enrollment 260 participants
Start Date 2026-08
Primary Completion 2027-12 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-07-21