Instant Flush Redness Clinical Efficacy Study
ConditionSensitive Skin
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-40
SponsorChinaNorm
About this trial
The goal of this clinical trial is to learn if an anti-redness emulsion can help lower facial redness caused by heat in healthy adult women. The main questions it aims to answer are:
* Does the anti-redness emulsion lower facial redness better than purified water? * Is the product safe and comfortable to use?
Researchers will compare the anti-redness emulsion to purified water using a split-face method.
Participants will:
* Receive infrared light on their face to trigger redness * Apply the anti-redness emulsion to one side of their face and purified water to the other side * Have their facial redness measured at different time points using photography, imaging devices, and skin redness tests * Answer questions about their experience with the products
Eligibility criteria
Qualifiers
Chinese women aged from 20-40 years old.
Self-declared mild sensitive skin.
Self-declare with skin concerns of redness and easy to flush.
Willing to be exposed to infrared light on the facial skin to induce facial redness(can tolerate heat sensation on the face).
Disqualifiers
Allergic to infrared light
Pregnant or breast-feeding woman or woman planning pregnancy during the study.
Subject deprived of rights by a court or administrative order.
Major subject to a guardianship order.
Trial design
Treatments tested in this trial
- Instant Anti-Redness Emulsion (FLA#2039188 43)
- Purified Water (Control)
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov