None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: •Volunteer (female and/or male) in generally good health. •Volunteer between the ages of 18 and 50 years. •Volunteer has not participated in a similar clinical investigation in the past three months. •Volunteer willing to give a written informed consent, agrees for audio video consenting procedures and come for regular observation. •Volunteer with clear back
Exclusion criteria
Exclusion criteria: •Known history or present condition of allergic response to any cosmetic products. •Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings. •Medications (e.g. steroids or antihistamines), which would compromise the study. •Known alcohol or drug abuse. •Pregnant or lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of Skin irritation potential (occurrence of Erythema, Oedema) w.r.t. the investigational products. Timepoint: For all the investigational products and positive control the subjects will be assessed by the study dermatologist on Day 1 (Day of patch application), Day 2 (0 hrs. of patch removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal), Day 9 (1 week after patch removal). | — |
Secondary
| Measure | Time frame |
|---|---|
| N/ATimepoint: N/A | — |
Countries
India
Contacts
AIM Research Services Pvt LTD.