None listed
Conditions
Interventions
Intervention1: 1.NYIS (serum)
2.NYIC (cream 1)
: All the subjects will be dermatologically and self assessed at pre product application (T0) and 15 minutes (T1) and 1 hour (T3) post application of in
Sponsors
Hindustan Unilever Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1.Volunteer in generally good health. 2.Volunteer between the ages of 25 and 35 years. 3.Volunteer has done salon visits two times in the last one year for cleanup and facial. 4.Volunteer with Fitzpatrick III or IV skin type. 5.Volunteer having visible significant open pores on face. 6.Volunteer has not participated in a similar clinical investigation in the past four weeks 7.Volunteer with no known allergy/ sensitivity to cosmetic products or fragrance and without any skin allergies / infections. 8.Volunteer not under any dermatologic treatment / prescribed medications. 9.Volunteer willing to abstain from using any cosmetic product on face, besides the provided product during the entire study course. 10.Volunteer willing to visit the site at specified frequencies for periodic evaluations. 11.Volunteer willing to comply with study specific requirements. 12.Volunteer willing to give a written informed consent and come for regular observation.
Exclusion criteria
Exclusion criteria: 1.A known history or present condition of allergic response to any cosmetic products. 2.Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings. 3.On medications (e.g. steroids or antihistamines), which would compromise the study. 4.Currently or has been undergoing dermatologist facial treatments or procedures within the last 1 month. 5.Volunteer; pregnant or nursing. 6.Volunteer viewed by the investigator as not being able to complete the study or participating in another study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of the study is to access efficacy of investigational product for itâ??s salon like tight & bright skin everyday on healthy human female subjects. Timepoint: All the subjects will be dermatologically and self assessed at pre product application (T0) and 15 minutes (T1) and 1 hour (T3) post application of investigational product. Instrumental evaluation will be carried out at pre product application (T0) and 1 hour (T2) & 2 hours (T4) post application of investigational product. As per randomization, either of the products will be allotted to all the subjects. Subjects will be asked to apply allotted investigational product on whole face. | — |
Secondary
| Measure | Time frame |
|---|---|
| The Secondary objective of this study is to access efficacy of investigational product for the Salon like lightening, Softness, Smoothness, Glow, Younger looking skin etc on the healthy human female subjects.Timepoint: All the subjects will be dermatologically and self assessed at pre product application (T0) and 15 minutes (T1) and 1 hour (T3) post application of investigational product. Instrumental evaluation will be carried out at pre product application (T0) and 1 hour (T2) & 2 hours (T4) post application of investigational product. As per randomization, either of the products will be allotted to all the subjects. Subjects will be asked to apply allotted investigational product on whole face. | — |
Countries
India
Contacts
Public ContactMs Aditi Barve
The KETs Scientific research centre, Cosmetology division
Outcome results
None listed