Clin2
NCT07432282Possibly a fitNot yet recruiting

Study of a new sensor for monitoring baby during labor induction

Induction of BirthCervical RipeningCervical Ripening and Induction of LaborBalloon Catheter for Labor Induction

Part of Women’s health & pregnancy clinical trials.

This trial tests a new sensor system (called INGA) to monitor your baby's heartbeat and your contractions during labor induction. It is for full-term pregnant women with an unripe cervix who are planning to have labor started using a balloon catheter.

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

Phase
N/A
Enrollment
120 people
Ages
18 years to 56 years
Study type
Interventional

Who can take part

  • You are at least 18 years old and pregnant with one baby.
  • Your pregnancy is at least 37 weeks (full term).
  • Your baby is head-down (not breech or sideways).
  • You have a cervix that is not ready for labor yet (Bishop score less than 6).
  • You have not had a C-section or any other uterine surgery before.
  • You do not have active infections, significant bleeding, or other serious health conditions.

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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