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A Study of Topical Steroids as Preemptive Therapy for EGFR Inhibitor-Induced Papulopustular Eruption | Clinical Trials | Clareo Health

TERMINATEDPHASE2

A Study of Topical Steroids as Preemptive Therapy for EGFR Inhibitor-Induced Papulopustular Eruption

A Randomized Phase II Study of Topical Steroids as Preemptive Therapy for Epidermal Growth Factor Receptor Inhibitor-Induced Papulopustular Eruption

NCT03115567•Northwestern University

View on ClinicalTrials.gov

Summary

This randomized, controlled, phase II clinical study is designed to assess the efficacy of preemptive treatment with topical steroids in preventing the papulopustular eruption induced by epidermal growth factor receptor inhibitor (EGFRI) treatment in cancer patients. Participants will be followed up for 6 weeks of twice daily application of triamcinolone cream to the face, chest, and back.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Patients must have a histologically or cytologically confirmed cancer diagnosis for which EGFRI treatment is indicated
•Initiation of topical steroids or control treatment within 3 days of initiation of cetuximab, erlotinib, panitumumab, or afatinib
•Patients must be age ≥ 18 years.
•Life expectancy of greater than 6 weeks
•Patient able to use topical medications reliably and complete questionnaires with assistance if needed
•Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study.

Exclusion Criteria

•Patients who have used systemic or topical steroids within 7 days of trial registration, or start systemic or topical steroids for reasons unrelated to trial during the 6-week follow up period
•Patients who have used antibiotics within 7 days of trial registration, or start antibiotics for other conditions during the 6-week follow up period
•History of allergic reactions to topical steroids
•Patients with any rash at the time of study registration
•Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
•Patients using any other topical medications in the treatment areas (face, chest, or back).

Locations (1)

Northwestern University Feinberg School of Medicine, Department of Dermatology

Chicago, Illinois, United States

Key Dates

Start Date

February 16, 2017

Primary Completion Date

April 24, 2020

Completion Date

September 2, 2022

Last Updated

May 17, 2023

Enrollment

ACTUAL participants

Conditions

Acneiform RashPapulopustular Eruption

Interventions

Triamcinolone

DRUG