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ENROLLING BY INVITATION
NCT05970354
PHASE4

EMLA Cream as Analgesic for Outpatient Gynecological Procedures

Sponsor: CAMC Health System

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to compare pain perception in the study participant population undergoing the following gynecological procedures: Intra Uterine Device (IUD) insertion, hysteroscopy, and endometrial biopsy and given either Eutectic Mixture of Local Anesthetics (EMLA) cream or a placebo. The main question to answer is: • Does EMLA cream reduce pain when administered during the following gynecological procedures: IUD insertion, hysteroscopy, and endometrial biopsy? Participants will be asked to do assess their pain on the Visual Analogue Scale through 3 times during the procedure. Researchers will compare the study group with those receiving placebo group to see if there is a difference in pain scores.

Official title: Lidocaine-Prilocaine Cream as Analgesic for Outpatient Gynecological Procedures; A Randomized-Control Trial

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

400

Start Date

2023-09-15

Completion Date

2025-02-28

Last Updated

2024-08-01

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

EMLA Cream

Eutectic Mixture of Local Anesthetics (Lidocaine 2.5% and Prilocaine 2.5%)

DRUG

VersaPro Cream Base for Compounding

Placebo

Locations (1)

Charleston Area Medical Center Institute for Academic Medicine

Charleston, West Virginia, United States