Status:
RECRUITING
Intrauterine Device Insertion Pain Management
Lead Sponsor:
University of Missouri-Columbia
Conditions:
IUD Insertion Pain
IUD Insertion
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
The goal of this clinical trial is to learn if use of topical benzocaine prior to the injection of lidocaine is effective in decreasing pain experienced during IUD insertion in patients 18 or older. T...
Detailed Description
The goal of the researchers is to determine if use of a topical benzocaine spray prior to lidocaine injection will cause a significant reduction in pain experienced by patients undergoing an IUD inser...
Eligibility Criteria
Inclusion
- 18 years of age or older
- Undergoing IUD insertion
Exclusion
- IUD insertion \<6 weeks postpartum
- Age \<18 years
- Allergy or history of adverse effect of lidocaine, benzocaine (and inactive ingredients: flavor, isobutane, propane, polyethylene glycol, sodium saccharin), or ibuprofen
- Not undergoing IUD insertion
- Undergoing IUD insertion under general anesthesia
- Usage of anti-inflammatory or as-needed anxiety medications (not daily use) in the 12 hours prior to IUD insertion
Key Trial Info
Start Date :
June 23 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
160 Patients enrolled
Trial Details
Trial ID
NCT06951191
Start Date
June 23 2025
End Date
December 1 2026
Last Update
July 8 2025
Active Locations (1)
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1
Missouri OB/GYN Associates-Smiley Lane
Columbia, Missouri, United States, 65202