drugset / Trial / NCT02961634

Study Efficacy and Safety in Comparative Use of Investigational Product Adjuvant Treatment in Onychomycosis

NCT02961634

RandomizedParallel-groupSingle-blindSupportive care

Summary

Single-center study, single blind, comparative with the objective of evaluating the efficacy and safety of an investigational product as an adjunct in the treatment of onychomycosis improvement of 90 days ± 2 days.

Timeline

Start
2017-04
Primary completion
2017-08
Completion
2017-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Ciclopirox Unknown 8 % Topical

Indications