Clinical Trial

Pain Control for Cervical Ripening Balloon

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
No standard of care exists for pain management during cervical ripening balloon placement. The purpose of this study is to evaluate if vaginal topical lidocaine reduces pain related to cervical ripening balloon placement during induction of labor.
Protocol Amendment History 1 change
critical Recruitment opened 2026-07-16
Trial Details
NCT Number NCT07268118
Lead Sponsor Beth Israel Deaconess Medical Center
Conditions Labor Induction
Enrollment 110 participants
Start Date 2026-05-13
Primary Completion 2027-06 (estimated)
Study Completion 2027-06 (estimated)
Updated on ClinicalTrials.gov 2026-07-15