A Clinical study to evaluate the efficacy of Khasa beeja tailam (Seed oil of Papaver somniferum) in Darunaka Vyadhi. - A Clinical study to evaluate the efficacy of khasa beeja tailam (Seed oil of Papaver somniferum) in Darunaka Vyadhi

Central council for Research in Ayurveda Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年8月21日

试验速览

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•1. Subjects in General good health of either sex. (Subjects without other specific health
•complaints.)
•2. Subjects within the age group of 18-55 years.
•3. Subjects willing to give a written informed consent and willing to abide by and
•comply with the study protocol.
•4. Subject exhibiting a slight to moderate dandruff or Seborrheic dermatitis of scalp on
•the total adherent and non adherent score after clinical examination, on Day 0.
•5. Subject having stopped any possible antidandruff treatment at least 2 weeks prior to

•1. Associated with other dermatological conditions such as psoriasis etc.
•Other Systemic illness.
•2. Pregnant, lactating mothers, menopausal women.
•3. Any Immuno-compromised patients and uncontrolled Diabetes
•4. Systemic treatment with corticosteroids, antibiotics, immune-suppressants etc, or any
•modern treatment within 3 months before of this trial.
•5. Subjects who have undergone hair growth treatment within 3 months before screening
•into the study. Subjects, who have history of alcoholism, smoking, crash dieting and/or
•psychiatric disorder including trichotillomania. Subjects who have had hair
•transplantation, who have taken pharmaceutical product which cause hirsutism(ex.phenytoin) and finasteride for androgenic alopecia, under medical treatment for
•hair problems.
•6. A known history or present condition of allergic response/hypersensitivity to any
•cosmetic ingredients and pharmaceutical products.
•7. Subjects on oral medications, undergoing any chemical hair salon treatmentstraightening / perming / colour / henna which will compromise the study.

发起方

Central council for Research in Ayurveda Sciences