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Clinical Investigation on the Efficacy and Safety of Relizema Ecofoam

Dermatitis Clinical Trial

Official title:
A Multicenter, Open Label, Uncontrolled Study for the Evaluation of Efficacy and Safety by Clinical Parameters of Relizema Ecofoam in Adult Atopic and Contact Dermatitis

Clinical Trial Summary

The scope of this open label clinical trial is to evaluate and confirm the performance of Relizema ecofoam in the improvement of the dermatitis severity. 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 Relizema 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 NCT05001139
Study type Interventional
Source Relife S.r.l.
Contact
Status Completed
Phase N/A
Start date November 15, 2021
Completion date June 15, 2023
View Details
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