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Clinical Investigation on the Performance and Safety of DermoRelizema Ecofoam

Dermatitis Clinical Trial

Official title:
Multicenter, Open Label, Uncontrolled Clinical Investigation on the Performance and Safety of DermoRelizema Ecofoam in the Management of Some Dermatitis in the Adult

Clinical Trial Summary

The scope of this open label clinical trial is to evaluate and confirm the performance of DermoRelizema ecofoam in the improvement of the dermatitis severity, by alleviating the symptomatology. The disease severity will be clinically measured through the Investigator Global Assessment (IGA) after 28 days of treatment.

Clinical Trial Description

The scope of this open label clinical trial is to evaluate and confirm the performance of DermoRelizema ecofoam in the improvement of the dermatitis severity, by alleviating the symptomatology. The product will be applied for 42 days of treatment, 2 times per day into the face. The dermatologist will perform 3 clinical follow up visits to assess the efficacy and safety of the product ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04826471
Study type Interventional
Source Relife S.r.l.
Contact
Status Completed
Phase N/A
Start date May 13, 2021
Completion date January 5, 2022
View Details
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