🏛️ Verified NIH Record • Updated 2026-05-04
Impact of Standardization on Outcomes Following Cervical Ripening (NCT07576881)
🟡 Not Yet Recruiting Phase2 / Phase3 💊 Investigational Drug / Biologic Sponsor: Indiana University
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Sidney & Lois Eskenazi Hospital — Indianapolis, Indiana
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Sidney & Lois Eskenazi Hospital — Indianapolis, Indiana
📞 Contact the Study Coordinator
Phone: (317) 880-2229
Email: semorgan@iu.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.