None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Subjects age group 18 - 55 years ? Healthy male & female volunteers ? Subjects with skin type III to V. ? Subjects willing to give a written informed consent. ? Subjects willing to maintain the patch test in position for 24 hours ? Subject has not participated in a similar investigation in the past two weeks. ? Subjects willing to come for regular follow up. ? Subjects ready to follow instructions during the study period.
Exclusion criteria
Exclusion criteria: ? Infection, allergy on the tested area ? Skin allergy antecedents or atopic subjects ? Hyper sensitivity to any component of the tested products ? Athletes and subjects with history of excessive sweating ? Cutaneous disease which may influence the study result ? Chronic illness which may influence the cutaneous state. ? Subjects on oral corticosteroid with dose 10mg/day ? Subjects participating in any other cosmetic or therapeutic trial. ? Any history of underlying uncontrolled medical illness including diabetes, liver disease or history of alcoholism, HIV or any other serious medical illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The objective of this study is to evaluate the dermatological safety of the given investigational product/s on skin of healthy human volunteers by dermatological visual assessment.Timepoint: 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
MS Clinical Research Pvt. Ltd