drugset / Trial / NCT01115244

Use of Dapsone Gel, 5% for Treating Dermatitis Herpetiformis

NCT01115244

Phase 4 Terminated 1 enrolled Vanderbilt University Medical Center
RandomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the efficacy of dapsone gel, 5% in the treatment of dermatitis herpetiformis. The primary efficacy end point will be the proportion of patients achieving success based on mean % reduction from baseline in total lesion counts at week six. Success for lesion reduction will be defined as statistically greater mean percent reductions at week six in the dapsone gel-treated extremity compared with the control extremity of each patient.

Timeline

Start
2010-07
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Dapsone Small molecule 5 % Topical