Evaluating Non-Invasive Measurement Tools to Differentiate Cellulite Affected Skin from Normal Skin on Healthy Human Volunteers

ITC R D Centre0 个研究点目标入组 10 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•Subjects willing to give written informed consent and abide by the study protocol.
•10 healthy female subjects in the age group of 20 to 50 yrs.
•At least 5 subjects with cellulite on at least one of the arms/ thighs and the remaining 5 with normal skin.
•Subjects with no medical history of disease / medical condition/ concurrent illness/ pre-existing or dormant dermatologic condition that could interfere with the study results.
•Subjects who are not pregnant or nursing.
•Subjects who are willing to abstain from using any cosmetic product on the identified sites on the day of study.

•Subjects who are pregnant or lactating.
•Subjects having skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations), which would interfere with the test readings.
•Subjects on medications (e.g. steroids or antihistamines), which could compromise the study results.
•Subjects with scars, cuts/ wounds/ scratches on the potential test sites (Brachium region, Femoral regions and Volar forearm), which could interfere with the test readings.

发起方