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Pain Control for Cervical Ripening Balloon

RecruitingPhase 2Ages 18 Years - anyFemaleBeth Israel Deaconess Medical Center
NCT07268118 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Age ≥18 years * Gestational age ≥37 weeks * Viable pregnancy * Intact membranes * English speaking * Interested in cervical ripening balloon placement * Able to provide consent Exclusion Criteria: * Allergy or sensitivity to lidocaine * Patients that already have neuraxial anesthesia (i.e. spinal, epidural, combined spinal/epidural) * Known uterine or cervical anomalies
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What it tests

  • topical vaginal application lidocaine gel
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Where

1 site
Beth Israel Deaconess Medical Center
Boston, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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