Health Condition 1: L659- Nonscarring hair loss, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Subjects with Hair loss problems,mild to moderate dandruff and thinning of hair. 2. Healthy Adult Volunteers of =18 to = 50 years inclusive of both genders 3. Subjects generally in good health and willing to give written informed consent and willing to follow the study procedure will be enrolled in the study 4. Subjects with hair all count of 40-50 for females and 25-30 for males as evaluated by 60secs comb test .
Exclusion criteria
Exclusion criteria: 1.History of any dermatological conditions of the scalp (other than dandruff or seborrheic dermatitis or hair loss) that would interfere with the diagnosis or assessment (e.g. psoriasis, eczema, atopic dermatitis, or other skin/scalp infections). 2. Subjects with excessive erythema, crusting or a significant number of pustules/papules on the scalp. 3. History ofskin cancer or treatment for any type of cancer within the last 2 years. 4. History of prior use of antidandruff treatment on scalp within past 1 month. 5. Participation in a similar clinical study within the previous 90 Days.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Evaluate the efficacy of the product for reducing hair fall. 2. Safety of the product in the treatment of dandruff. 3. Evaluating the efficacy and safety of product on increasing the hair growth or reducing the thinning of HairTimepoint: Baseline,Day 14,Day 30,Day 60 | — |
Secondary
| Measure | Time frame |
|---|---|
| NATimepoint: NA | — |
Countries
India
Contacts
Trial Guna Pvt Ltd