Clinical Trial

Empathy Through Pain Control: Lidocaine Paracervical Block for IUD Placements

Study acronym: EPIC
Recruiting
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Summary
The goal of this research study is to learn more about how different uses of a numbing medication might affect pain levels while getting an IUD placed. The investigators are also studying participants opinions of their clinicians' empathy. The investigators are inviting patients who arrive at their clinic visit seeking an IUD. Usually, at University of California, San Diego (UCSD), for patients who have never delivered a baby, clinicians use a buffered paracervical block for before IUD placement. The purpose of this research study is to investigate whether a "buffered" (2 cc of sodium bicarbonate, 18 cc of 1% lidocaine) paracervical block (numbing medication given on both sides of the cervix) is effective in reducing pain during IUD placement in individuals with prior C-sections, the difference between buffered and unbuffered for nulliparous patients, and whether a medicated gel reduces pain with the paracervical block.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-04-28; most recent amendment 2025-06-10.
Status change: Not Yet Recruiting → Recruiting 2025-06-10
Trial Details
NCT Number NCT06960317
Lead Sponsor University of California, San Diego
Conditions Contraception, Pain, Acute, Anesthesia, Local
Enrollment 204 participants
Start Date 2025-06-04
Primary Completion 2027-06-30 (estimated)
Study Completion 2028-06-30 (estimated)
Updated on ClinicalTrials.gov 2025-06-13