drugset / Trial / NCT06974019

Empathy Through Pain Control: Buffered Compared to Unbuffered 1% Lidocaine During IUD Placement

NCT06974019

Not yet recruiting 68 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 patients' opinions of their clinicians' empathy. The investigators are inviting patients who have never given birth who arrive at their clinic visit seeking an IUD. Usually, at University of California, San Diego (UCSD), for patients who have never delivered, clinicians numb both the sides of the cervix with a lidocaine-based paracervical block. The purpose of this research study is to compare perceptions of pain between buffered (2 cc of sodium bicarbonate, 18 cc of 1% lidocaine) vs. unbuffered paracervical block (20 cc 1% lidocaine) during IUD placement for nulliparous women.

Timeline

Start
2025-06-01
Primary completion
2027-06-30
Completion
2028-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine Other / unclassified 18 ml Other
Subject Lidocaine Other / unclassified 20 ml Other
Subject sodium bicarbonate Diagnostic / imaging agent 2 ml Other

Indications

No indication recorded.