Clin2
NCT06506721Possibly a fitRecruiting

Comparing two devices for labor induction after one C-section

Delivery, ObstetricCesarean SectionObstetric Delivery

Part of Women’s health & pregnancy clinical trials.

This study compares two medical devices used to start labor in women who have had one previous C-section and whose cervix is not yet ready. It aims to find which device works best for safely inducing labor.

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

Phase
N/A
Enrollment
137 people
Ages
18 years to 60 years
Study type
Interventional

Who can take part

  • You are 18 or older and have had exactly one previous C-section (not more than one).
  • You are between 24 and 42 weeks pregnant and your doctor decides labor needs to be induced.
  • Your cervix is not yet soft or open (a Bishop score less than 6).
  • You are not pregnant with twins, and the baby is not in a breech or sideways position.
  • You do not have certain complications like infection, bleeding, placenta problems, or a history of other uterine surgeries.

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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