Dermatological Evaluation of Safety & Efficacy of Bath Accessories OnHealthy Human Subjects - NI

ITC Life Sciences Technology Centre0 sites24 target enrollmentTBD

Overview

No summary available.

Registry

who.int

Start Date

TBD

End Date

December 13, 2017

Last Updated

3 years ago

Study Type

Interventional

Sponsor

ITC Life Sciences Technology Centre

•1\.Male and female volunteers in the age group of 18 to 50 years.
•2\.A total of 48 Male and 24 Female subjects.
•3\.Nearly equal representation of all skin typesÃ¢â?¬â?? Normal, Dry, Oily, Combination, Sensitive skin.
•4\.Female Volunteers who are neither pregnant nor nursing.
•5\.Volunteers having experienced a liquid bathing product in the past 6 months.
•6\.Volunteers who are willing to abstain from using any product other than the provided test products during the study period.
•7\.Volunteers willing to give a written informed consent.

•1\.Volunteers with an active skin disorder or a significant history of skin disorders (e.g. psoriasis, eczema, vitiligo, pityriasis versicolor, acne) which in the opinion of the Principle Investigator or Dermatologistmay affect the test results.
•2\.Volunteers whose skin has been excessively exposed to Sun or UV rays during the previous month in the opinion of the Investigator.
•3\.Volunteers with a known history or current condition of allergy or sensitivity to cosmetic products/fragrances.
•4\.Volunteers on undergoing any medical treatment or taking any systemic medicines since or taking steroids or antihistamines or medicines for chronic medical conditions or applying any topical medication that could compromise the study.
•5\.Female volunteers who are currently pregnant or breastfeeding.
•6\.Volunteers participating in any other cosmetics or any other clinical trial