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Clinical Trial

3-hour Versus 12-hour Double-balloon Catheter for Labor Induction

NCT: NCT07492186 · NOT_YET_RECRUITING

NCT IDNCT07492186
StatusNOT_YET_RECRUITING
Start Date2027-03-01
Completion2027-03-15

Brief Summary

This study aims to demonstrate that a 3-hour ultra-short cervical ripening protocol using a double-balloon catheter significantly reduces the induction-to-birth interval by at least 6 hours compared to the standard 12-hour protocol. The study evaluates whether this reduction can be achieved without increasing cesarean section rates or maternal-fetal risks

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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