Clinical Trials Directory

Trials / Completed

CompletedNCT01429701

Effectiveness of Polymyxin B Sulphate + Prednisolone + Benzocaine + Clioquinol in Acute and Sub-acute Dermatitis Eczematous

Unicentric Comparing Effectiveness of Polymyxin B Sulphate + Prednisolone + Benzocaine + Clioquinol to Betamethasone + Gentamicin + Tolnaftate + Clioquinol in Acute and Sub-acute Dermatitis Eczematous

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
76 (actual)
Sponsor
EMS · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Dermatitis eczematous is a recurrent pruritic skin disorder which has a significant morbidity and impaired quality of life due specially pruritus and physical visible skin lesions. The purpose of this trial is evaluate the effectiveness of two different topic associations of drugs.

Detailed description

Study design: * Experiment duration: 22 days * 2 visits (days 0,7,15 and 22) * Reducing eczema area and severity index evaluation * Adverse events evaluation * Double blinded, non-inferiority, prospective parallel-group, intend to treat trial.

Conditions

Interventions

TypeNameDescription
DRUGpolymyxin B sulphate + prednisolone + benzocaine + clioquinolapplied 3 times / day at lesion
DRUGbetamethasone + gentamicin + tolnaftato + cleoquinolapplied 3 times / day at lesion

Timeline

Start date
2012-05-01
Primary completion
2012-06-01
Completion
2012-08-01
First posted
2011-09-07
Last updated
2021-02-24

Source: ClinicalTrials.gov record NCT01429701. Inclusion in this directory is not an endorsement.