Evaluation of Skin Safety of test products using 24 Hours Patch Test Under CompleteOcclusion on Adult Healthy Human Participants with Normal Skin. IS 4011:2018 Guidelines. - NI

Dabur Research and Development Centre.0 个研究点目标入组 26 人开始时间: 待定最近更新: 2024年1月22日

试验速览

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•1. Voluntary men and women (preferably equal number of males and females) between 18
•and 65 years.
•2. Participants representing normal, oily, dry and combination skin type in equal ratio.
•3. Fitzpatrick skin type III to IV.
•4. Having apparently healthy skin on test area.
•5. Willingness to discontinue the use of cleansing and/or cosmetic products in the application
•areas during the course of the trial
•6. Cooperating, informed of the need and duration of the examinations, and ready to comply
•with protocol procedures.
•7. Willing to give written informed consent to participate in the trial after informing all
•information concerning the trial procedures and trial objectives.
•8. Willingness to avoid intense UV exposure on test site (sun or artificial UV), during the
•course of the trial.
•9. Willingness to avoid water contact (i.e.: swimming) or activity which cause sweating (i.e.:
•exercise, sauna...), during the course of the trial.
•10. Should be able to read and write (in English, Hindi, or local language).
•11. Ready to wear loose cotton clothes
•12. Having valid proof of identity and age.
•13. Subject having not participated in another trial in the past one month.

•1. Pregnancy (by history) and lactating women.
•2. Scars, excessive terminal hair, tattoo, cuts, wounds, irritation symptoms, abrasion or any
•other skin condition on the studied area.
•3. Athletes and subjects with history of excessive sweating
•4. Subjects on oral corticosteroid
•5. Any history of underlying uncontrolled medical illness including diabetes, liver disease or
•history of alcoholism, HIV or any other serious medical illness.
•6. A participant who the Investigator feels will not be compliant with trial requirements
•7. Dermatological infection/pathology on the level of studied area.
•8. Hypersensitivity, allergy antecedent (to any cosmetic product, raw material, hair dye).
•9. Any clinically significant systemic or cutaneous disease, which may interfere with trial
•procedures.
•10. Chronic illness which may influence the outcome of the trial.
•11. Participants on any medical treatment either systemic or topical which may interfere with
•the performance of the trial (presently or in the past 1 month).
•12. Participant in an exclusion period or participating in another food, cosmetic or therapeutic

发起方

Dabur Research and Development Centre.