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Study Reference No. - C3F00602

Demographic Gender Age Location Compensation
50% to have normal skin, 50% to have dry skin, 50% overall to self-report sensitive skin Female 18-65 Winnipeg, MB $242
Study Details

Study Purpose

The purpose of this study is to determine the mildness and moisturization of personal washing cleanser by visual evaluation for dryness and erythema in combination with non- invasive instrumental hydration and skin barrier evaluations through controlled application technique.Up to 65 Female participants will participate in the conditioning phase of the study and of these, approximately 45 healthy women, ages 18 through 65 will participate in the product application phase of the study.

Study Duration

Total 11 Visit
Screening, product application and assessment phase

Study Schedule

General Screening

November 26th, December 8th

Medical Screening

N/A

Study Visit(s)

Visit 1 (approx. 1 hour)
Informed Consent, medical history, inclusion/exclusion questions.

Visit 2 (approx. 2 hours)
Medical history, sit for 20 min in environmental controlled room prior to visual, instrumentation (Corneometer, Skicon and TEWL). Lastly product application.

Visit 3, 5, 7 and 9 (approx. 1 hour on each visit)
sit for 20 min in environmental controlled room prior to visual, instrumentation (Corneometer, Skicon).

Visit 4, 6, 8 and 10 (approx. 1.5 hours on each visit)
sit for 20 min in environmental controlled room prior to visual, instrumentation (Corneometer, Skicon). Lastly product application.

Visit 11 (approx. 1.25 hours)
sit for 20 min in environmental controlled room prior to visual, instrumentation (Corneometer, Skicon and TEWL).

Follow-Up Visit(s)

N/A

Other Notes

Bring valid ID

May be excluded if skin type is not as per study requirement.