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Completed NCT05970354

EMLA Cream as Analgesic for Outpatient Gynecological Procedures

Conditions: Pain

Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: Yes
Phase: PHASE4
Enrollment: 31
Sponsor: CAMC Health System

Location: Charleston Area Medical Center Institute for Academic Medicine Charleston West Virginia

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.

Eligibility Criteria

Inclusion Criteria: * Patient will undergo one of the following procedures: intra-uterine device insertion, hysteroscopy, or endometrial biopsies Exclusion Criteria: * Known hypersensitivity to amide anesthetics * Pre-existing methemoglobinemia

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05970354). StuddyBuddy aggregates publicly available trial information.