U.S., July 9 -- ClinicalTrials.gov registry received information related to the study (NCT07689357) titled 'Cervical Ripening Balloon, 3 Hours vs 12 Hours Placement' on June 30.
Brief Summary: The goal of this clinical trial is to learn if a shorter duration of cervical ripening balloon (CRB) placement can reduce the time to delivery in pregnant women undergoing induction of labor.
The main questions it aims to answer are:
Does placing the cervical ripening balloon for 3 hours or less result in a shorter interval from insertion to delivery compared to the standard 12-hour placement?
Does a shorter 3-hour balloon placement lead to better pregnancy outcomes, fewer complications, and lower maternal discomfort?
Researchers will compare a g...