Pain Control for Cervical Ripening Balloon
Recruiting
Phase 2
Interventional Study
Labor Induction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 110 (estimated)
- Sponsor
- Beth Israel Deaconess Medical Center · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
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.
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
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 a…
Contacts