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NOT YET RECRUITING
NCT06974019
NA

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

Sponsor: University of California, San Diego

View on ClinicalTrials.gov

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.

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

68

Start Date

2025-06-01

Completion Date

2028-06-30

Last Updated

2025-05-15

Healthy Volunteers

Yes

Interventions

DRUG

Buffered Lidocaine

To determine if a 20 cc buffered (2 cc of sodium bicarbonate, 18 cc of 1% lidocaine) lidocaine paracervical block decreases pain with IUD placement in nulliparous women

DRUG

Lidocaine 1% Injectable Solution

To determine if the unbuffered 1% lidocaine paracervical block offers any less pain control with IUD placement for nulliparous women