Evaluation of anti-dandruff Efficacy of Test products On Healthy Human Subjects
- Registration Number
- CTRI/2017/05/008658
- Lead Sponsor
- ITC LIMITED ITC Life Sciences and Technology Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 47
1 Healthy Indian / Asian male and female subjects in the age group of 20-45 yrs.
2Subjects who are willing to give signed informed consent and who consent to abide by the study protocol and restrictions for the entire study duration.
3 Subjects with hair of sufficient length that allows parting of scalp hair into clear sections for scalp examination.
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 (Dermatologistââ?¬•s scoring based on subjectââ?¬•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).
Subjects with a known history or present condition of allergic response to any shampoo or conditioner.
1 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.
2 Subjects with severe hair fall due to endocrine disorders as diagnosed by dermatologist or revealed through oral interview.
3 Subjects on medications (steroids, antihistamines, antimicrobials), which would compromise the study results (Subjects inputs).
4 Subjects with very short hair as in those sporting Crew cut or near tonsured scalps.
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 undergoing therapy for dandruff (Subjects inputs).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method OutcomeAnti-Dandruff Efficacy of Test products On Healthy Human Subjects Based on Half Head Application DesignTimepoint: OutcomeAnti-Dandruff Efficacy of Test products On Healthy Human Subjects Based on Half Head Application Design
- Secondary Outcome Measures
Name Time Method ot ApplicableTimepoint: Not Applicable