Clin2
NCT07576881Likely a fitNot yet recruiting

Improving labor induction outcomes with standardized cervical ripening

Pregnancy

Part of Women’s health & pregnancy clinical trials.

This study tests whether using a standardized approach to preparing the cervix for labor induction leads to better outcomes. You would be randomly assigned to receive either a medication (misoprostol) or a small balloon device to soften and open your cervix before labor is induced.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2/Phase 3
Enrollment
1,158 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are pregnant and scheduled for labor induction at Eskenazi Hospital
  • You are at least 37 weeks pregnant (full term or near full term)
  • You are 18 years or older
  • You can read, speak, and understand English, Spanish, or Haitian Creole
  • You do not have certain pregnancy conditions (like placenta previa, ruptured membranes, or a previous cesarean scar)
  • You need cervical ripening (your cervix is not yet ready for labor)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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