RecruitingPhase 2NCT07268118

Pain Control for Cervical Ripening Balloon

Randomized Control Trial for Pain Control With Topical Lidocaine for Cervical Ripening Balloon Placement


Sponsor

Beth Israel Deaconess Medical Center

Enrollment

110 participants

Start Date

May 13, 2026

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called topical vaginal application lidocaine gel for people with labor induction. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGtopical vaginal application lidocaine gel

Application of topical vaginal lidocaine prior to cervical balloon ripening


Locations(1)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

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NCT07268118


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