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: 24HRS, 48HRS, 1 WEEK | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
MS Clinical Research Pvt. Ltd