RecruitingPhase 2NCT06223659

EMLA Topical Cream for Treatment of Pain in Patients Receiving Intra-Dermal Technetium 99 Injections for Lymphoscintigraphy for Skin Cancers

Investigating the Use of EMLA Topical Cream for Patients Receiving Intra-Dermal Technetium 99 Injections for Lymphoscintigraphy for Cutaneous Cancers


Sponsor

Ohio State University Comprehensive Cancer Center

Enrollment

100 participants

Start Date

Dec 19, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial tests how well EMLA topical cream works in treating pain in patients with skin cancers receiving Technetium 99 injections for a lymphoscintigraphy mapping procedure. A lymphoscintigraphy mapping procedure is used to find the main or lead lymph node (tissue that fight infection) so it can be removed and checked for tumor cells. Using lymphoscintigraphy to highlight and then surgically remove lymph nodes is standard way to treat skin cancer for many patients. The Technetium 99 injections used for lymphoscintigraphy can be briefly painful due to the sensitivity of the nerve endings in the skin. The EMLA topical cream, which contains a numbing medicine to block pain from nerve endings, has been studied in breast cancer patients with a difference in pain reported, but this is the first time it has been studied in patients undergoing lymphoscintigraphy for skin cancer. This study may help researchers learn whether the use of EMLA cream may improve the associated pain at the time of the lymphoscintigraphy procedure.


Eligibility

Min Age: 18 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether EMLA numbing cream applied to the skin before radioactive tracer injections (used to map lymph nodes before skin cancer surgery) reduces pain during the procedure. **You may be eligible if...** - You are between 18 and 99 years old - You have been diagnosed with a skin cancer (melanoma, Merkel cell carcinoma, squamous cell carcinoma, or other skin malignancy) - You are scheduled for lymph node mapping and sentinel lymph node biopsy as part of your cancer care **You may NOT be eligible if...** - You have a known allergy to EMLA cream, lidocaine, prilocaine, or any local anesthetic - You have an allergy to adhesives - You are pregnant - You have a pre-existing chronic pain condition (as defined by the CDC) or have taken narcotic pain medications in the 7 days before the procedure - You are incarcerated or unable to independently provide consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEutectic Mixture of Local Anesthetics

Apply topically to skin

DRUGPlacebo Administration

Apply topically to skin

OTHERQuestionnaire Administration

Ancillary studies


Locations(1)

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

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NCT06223659


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