Evaluation of the Effect of Combined Use of Cosmetic Products for Dry and Itchy Skin.
ConditionDry Skin
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorLacer S.A.
About this trial
The goal of this study is to learn if combined use of shower oleogel and body lotion works to improve skin itching and dryness in adults. It will also learn about its safety. The main question it aims to answer is:
• Does the products use improves skin hydration and itching? Researchers will compare shower oleogel and body lotion to a commercially available shower gel and the body lotion to see if the combined use is more efficient than use of body lotion alone.
Participants will:
* Use assigned products every day for 1 month * Visit the CRO for checkups and tests on established schedule
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age: 18-70 years old
Gender: both
Sensitive skin and 30% to 50% with atopic tendency (scored 8-12)
With dry or very dry skin on the body
Disqualifiers
cutaneous marks on the experimental areas, which could interfere with the assessment of skin reactions (pigmentation troubles, scar elements, over-developed pilosity, ephelides and naevi in too great quantity, sunburn),
allergy or reactivity to products of the same category than the tested one,
with history of malignant melanomas (Dubreullh melanosis…)
unbalanced hormonal treatment,
Trial design
Design model
Parallel
Treatments tested in this trial
Shower oleogel and body lotion
Other interventionDaily use of shower oleogel and body lotion for 28 days
Shower gel and body lotion
Other interventionDaily use of shower gel and body lotion
Treatment groups
60 Participants
are divided into 2 treatment groupsGroup A: shower oleogel and body lotionExperimental treatment 1 intervention
Group B: shower gel and body lotionActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Change from Baseline in the rate of skin hydration (capacitance measured by Corneometer) at 4 weeks
Time frame
From enrollment to the end of the study at 4 weeksSecondary outcomes
1
Change from Baseline in the rate of skin barrier function (TEWL evaluated by Tewameter) at 4 weeks.
Time frame
From enrollment to the end of the study at 4 weeks Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: