None listed
Conditions
Interventions
Intervention1: Face & Body Lotion: Approx. 50 mg, Neat, Single application on volar forearms
Intervention2: Face & Body Cream: Approx. 50 mg, Neat, Single application on volar forearms
Intervention3
Sponsors
NMantra
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy males and non-pregnant/non-lactating females (Preferably equal ratio) with age 18 to 50 years (both inclusive at the time of consent). 2. Participants having good general health as determined by the Investigator on the basis of medical history. 3. Female participants of childbearing potential must have a negative urine pregnancy test performed at enrollment visit. 4. Participants who are willing to abstain from using any cosmetic product on test sites during the course of the study. 5. Participants who are willing to participate in the study and give signed consent. 6. Participants should be willing and able to follow the study protocol to participate in the study Participants with intact, healthy skin at the designated test sites, free from cuts, abrasions, active dermatoses, or dermatological conditions. 7. Participants willing to follow all the acceptable forms of contraception as applicable.
Exclusion criteria
Exclusion criteria: 1. Participants using Body milk /lotion / cream, cosmetics or any other body moisturizing product 3-5 days prior to study. 2. Participants who are on systemic medication or any medications would compromise the study. 3. Chronic illness which may influence the cutaneous state. 4. Participants having a history of diabetes. 5. Participants with known allergy or sensitivity to cosmetic products and/or any ingredients of the test product. 6. Participants with medical history (past/present) of significant dermatological diseases or conditions, such as atopy, psoriasis, vitiligo or other conditions known to alter skin appearance or physiologic response (e.g., porphyria) chronic urticaria, or sunburn, rashes. 7. Participant having skin irritation, blemishes, excessive hair, moles, pigmentation, pimples, marks (e.g., tattoos, scars, and sunburn), open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the test site(s) i.e., volar forearm that can interfere with the reading. 8. Participants participating in a similar clinical study, currently or within the last four weeks. 9. Any participants, in the Investigator opinion not considered suitable for enrollment. 10. Any other condition which could warrant exclusion from the study, as per the Dermatologist s/investigator s discretion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Instrumental and Dermatological AssessmentTimepoint: Day 01 [(Before application (i.e., baseline) and after application at 01 hour (plus 15 mins), 04 hours (plus 15 mins) and 6 hours (plus 15 mins)] and on Day 02 [24 hours (plus 15 mins) after application]. | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective EvaluationTimepoint: Day 02 [24 hours plus 15 mins) after application]. | — |
Countries
India
Contacts
Public ContactDr Parth Joshi
Cliantha Research
Outcome results
None listed