None listed
Conditions
Interventions
Intervention1: Test product A: Face cream: Dose: 0.6 gm
Dosage Form: Cream
route of administration: topical
frequency: twice a day
mode of usage: Apply a coin sized (Approx. 0.6gm) amount of the test
Sponsors
S H Kelkar and Company Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1)Age: 30 to 55 years (both inclusive) at the time of consent. 2)Sex: Adults female having Crow s feet area wrinkles and fine lines. 3)Females of childbearing potential should have a self-reported negative urine pregnancy test at the time of screening visit. 4)Subjects should not have used any cosmetic, nutraceutical or therapeutic products for skin ageing in last 6 months. 5)Subjects must be willing to stop using any cosmetics or any medical products for skin ageing for the duration of the study. 6)Subjects are not allowed to participate in any other study until this study is complete. 7)Subjects must be willing and able to follow the study directions and to return for all specified visits with the product. 8)Subjects must agree to record each use of the test products in the subject s diary card on daily basis. 9)Subjects must agree to record medication use during the study.
Exclusion criteria
Exclusion criteria: 1)Subjects who are on steroids for last six months. 2)Subjects who have used any cosmetic, nutraceutical or therapeutic products for skin last six months. 3)Subjects who are on product which contains kojic acid, glycolic acid, niacinamide, alpha arbutin, Vitamin C and other skin ageing product. 4)Subjects with other dermatologic diseases whose presence or treatments could interfere with the assessment of study. 5)Subjects that are pregnant and/or breastfeeding. 6)The subject has a known allergy or sensitivity to soaps, lotions, detergents, detanglers or fragrances. 7)Subjects if do not agree to limit sun exposure to affected areas such as face during prolonged sun exposure. 8)The subject has any other skin conditions i.e. cuts, scratches, ring worms, etc. which in the opinion of the Investigator, will interfere with the study results or will create undue risk for the subject. 9)The subject has any of the conditions or factors that the Investigator believes may affect the response of the skin or the interpretation of the test results. 10)The subject is currently taking or has taken any medication, which the Investigator believes may influence the interpretation of the data. 11)Any other condition which could warrant exclusion from the study, as per the dermatologist s/investigator s discretion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To evaluate the effectiveness of the test products in terms of change in skin elasticity from baseline before usage and after usage of the test products, and between test products by using Cutometer. 2.To evaluate the effectiveness of the test products in terms of change in skin texture i.e. skin roughness, smoothness, scaliness, wrinkles, and fine lines from baseline before usage and after usage of the test products, and between test products by using VISIOSCAN VC 20 Plus. Timepoint: On Day 01, on Day 30 and Day 60 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To evaluate the effectiveness of the test products in terms of changes in wrinkles and finelines from baseline before usage and after usage of the test products, and between test products by using scoring scale. Timepoint: On Day 01,on Day 30 and Day 60;2.To evaluate the effectiveness of the test products in terms of subjective product perception and non-comedogenic questionnaire assessment by using scoring scaleTimepoint: On Day 01, on Day 30 and Day 60 | — |
Countries
India
Contacts
Public ContactMaheshvari N Patel
NovoBliss Research Private Limited
Outcome results
None listed