drugset / Trial / NCT06960317

Empathy Through Pain Control: Lidocaine Paracervical Block for IUD Placements

NCT06960317 ↗

Recruiting 204 enrolled University of California, San Diego
RandomizedParallel-groupSingle-blindTreatment

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.

Timeline

Start
2025-06-04
Primary completion
2027-06-30
Completion
2028-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine Other / unclassified 1 % Other
Subject Lidocaine Other / unclassified 2 % Other
Subject Lidocaine Other / unclassified 20 ml Other

Indications

No indication recorded.