Evaluating Anti dandruff Efficacy of Hair Leave on Products on Healthy Human Subjects Based on Half Head Application Design. - NI

ITC Life Science and Technology Centre0 个研究点目标入组 39 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•1.Subjects who are willing to give signed informed consent and who consent to abide by the study protocol and restrictions for the entire study duration.
•2.A mixed population of healthy male and female subjects in the age group of 20-45 yrs.
•3.Subjects with preferably lengthy hair (for female subjects) but not mandatory.
•4.Subjects with moderate to severe scalp dandruff score (with dandruff on both sides of the scalp).
•5.Subjects with moderate to severe scalp itch score (Scoring based on subjectâ??s feedback)
•6.Subjects who have not participated in a similar investigation in the past four weeks.
•7.Subjects who are not sensitive to the ingredients of the test product (As disclosed by the subjects or as observed during the Skin sensitivity test).

•1.Subjects with a known history or present condition of allergic response to any shampoo or conditioner.
•2.Subjects having communicable skin/scalp infections or other skin disease (e.g. psoriasis, atomic dermatitis or other cutaneous manifestations), which could interfere with the test results as diagnosed by Dermatologist.
•3.Subjects with severe hair fall due to endocrine disorders as diagnosed by dermatologist or revealed through oral interview.
•4.Subjects on medications (steroids, antihistamines, antimicrobials), which would compromise the study results (Subjects inputs).
•5.Female subjects who are pregnant (determined by Urine pregnancy test), lactating, or planning pregnancy during the course of the study (Subjects inputs).
•6.Subjects with signs and symptoms of systemic and / or chronic illness (As diagnosed by Dermatologist)
•7.Subjects who are regular users of anti- dandruff shampoo/ undergoing therapy for dandruff (Subjects inputs).

发起方

ITC Life Science and Technology Centre