This is a monocentric, open and randomized study. The purpose is to evaluate the cutaneous tolerance of three medical masks (class I medical device) after 3 consecutive days of use on a population with normal or sensitive skin.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
98
During 3 consecutive days
Laboratoire Eurofins Dermscan Pharmascan
Villeurbanne, France
Cutaneous tolerance
Evaluation of the percentage of subjects presenting no relevant clinical or functional signs of cutaneous intolerance after 3 days of use of the three medical devices
Time frame: Days 3
Subjective appreciation
Analysis of the subject's answer to a subjective evaluation questionnaire
Time frame: 3 days
Number of Adverse event
Collection of cutaneous and systemic Adverse Event
Time frame: 3 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.