Clinical evaluation of Khasa beeja tailam external application (Seed oil of Papaver somniferum Linn.) in the cases suffering with Dandruff.

Phase 2

• Conditions: Health Condition 1: L210- Seborrhea capitis

• Registration Number: CTRI/2023/05/052349
• Lead Sponsor: Central council for Research in Ayurveda Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

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

Day 0.

Exclusion Criteria

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified