None listed
Conditions
Interventions
Intervention1: Marketed Test Product: Topical Application Frequency: Single Application Spread the cream in the same direction.
Control Intervention1: Control Product: Topical Application Frequency:
Sponsors
NovoBliss Research Private Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age: 18 to 55 years old (both inclusive) at the time of consent. 2) Sex: Healthy male and non-pregnant/non-lactating females. 3) Subject having normal, dry and sensitive skin. 4) Females of childbearing potential must have a self-reported negative pregnancy test. 5) Subject are generally in good health. 6) Subject is able to remain on stable doses of contraceptive or replacement hormonal therapy, including no therapy, 6 weeks prior to and for the duration of the study. 7) If the subject is of childbearing potential, is practicing and agrees to maintain an established method of birth control (IUD, hormonal implant device/injection, regular use of birth control pills or patch, diaphragm, condoms with spermicide or sponge with spermicidal jelly, cream or foam, partner vasectomy or abstinence). Females will be considered as non-childbearing potential if they are surgically sterile, have been post-menopausal for at least 1 year or have had a tubal ligation. 8) Subjects are willing to give written informed consent and are willing to come for regular follow up. 9) Subjects who commit not to use any other skincare products for the entire duration of the study. 10) Subject who has not participated in a similar investigation in the past three months. 11) Willing to use test product throughout the study period.
Exclusion criteria
Exclusion criteria: 1) History of any dermatological condition of the skin diseases. 2) Subject with present condition of allergic response to any cosmetic product. 3) Subject having allergic response to the ink. 4) Subjects under chronic medication (e.g. aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy etc.) that might influence the outcome of the study. 5) Subjects who have applied topical treatment for at least 4 weeks and any systemic treatment for at least 3 months, before they participated in the study. 6) History of alcohol or drug addiction. 7) Subjects using other marketed products during the study period. 8) Any other condition which could warrant exclusion from the study, as per the dermatologist s/investigator s discretion. 9) Pregnant or breastfeeding or planning to become pregnant during the study period. 10) History of chronic illness which may influence the cutaneous state. 11) Subjects participating in other similar cosmetics, devices or therapeutic trials or skincare products within the last four weeks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To observe the effects of ceramide-containing moisturizer versus water application on skin parameters: Skin Glow and least reflection factor Skin Glossymeter GL 200 Skin Hydration Corneometer CM 825 TEWL Tewameter TM Hex Skin Smoothness, Roughness, Skin Scaliness VisioScan VC 20 Plus. Sebum Level Sebumeter SM 825 Timepoint: At baseline (before application) and at post-application at T15 mins. | — |
Secondary
| Measure | Time frame |
|---|---|
| To examine correlations between the least-reflection factor particularly hydration & skin surface shine to evaluate its potential utility as an integrated indicator of skin reflection factorTimepoint: At baseline & post-application at T15 mins. | — |
Countries
India
Contacts
Public ContactMaheshvari Patel
NovoBliss Research Pvt. Ltd.
Outcome results
None listed