drugset / Trial / NCT04290572

Efficacy and Safety of Oral Isotretinoin for the Treatment of Facial Recalcitrant Flat Warts

NCT04290572

RandomizedParallel-groupDouble-blindTreatment

Summary

Randomized clinical trial to compare the efficacy of different doses of oral isotretinoin 10 mg/day, 20 mg/day and 30 mg/day during 12 weeks for the treatment of facial recalcitrant flat warts. The primary endpoint will be the proportion of participants with total remission of facial flat warts at the end of the intervention in the three arms of the clinical trial.

Timeline

Start
2020-03-15
Primary completion
2023-02-28
Completion
2023-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Isotretinoin Other / unclassified 10 mg Oral
Subject Isotretinoin Other / unclassified 20 mg Oral
Subject Isotretinoin Other / unclassified 30 mg Oral

Indications