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
| Type | Name | Description |
|---|---|---|
| DRUG | polymyxin B sulphate + prednisolone + benzocaine + clioquinol | applied 3 times / day at lesion |
| DRUG | betamethasone + gentamicin + tolnaftato + cleoquinol | applied 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.