Trials / Not Yet Recruiting
Not Yet RecruitingNCT07268118
Pain Control for Cervical Ripening Balloon
Randomized Control Trial for Pain Control With Topical Lidocaine for Cervical Ripening Balloon Placement
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 110 (estimated)
- Sponsor
- Beth Israel Deaconess Medical Center · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | topical vaginal application lidocaine gel | Application of topical vaginal lidocaine prior to cervical balloon ripening |
Timeline
- Start date
- 2026-04-01
- Primary completion
- 2027-06-01
- Completion
- 2027-06-01
- First posted
- 2025-12-05
- Last updated
- 2026-03-05
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07268118. Inclusion in this directory is not an endorsement.