None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Female participants aged between 18 and 55 years. Individuals presenting clinical symptoms of hair loss, hair thinning, scalp dryness, or decreased hair tensile strength. Participants willing to avoid concurrent use of other topical or systemic hair treatments throughout the study period. Ability to understand the study requirements and provide written informed consent.
Exclusion criteria
Exclusion criteria: Active scalp infections or dermatological disorders such as seborrheic dermatitis, psoriasis, or tinea capitis. Known hypersensitivity to any botanical extract or coconut-based oil used in the product. Current use of systemic or topical pharmacological treatments for alopecia (e.g., minoxidil, corticosteroids, finasteride). Pregnant or lactating women. Participation in another clinical study or investigational drug/product trial within the preceding 30 days.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| TimePoints 1. Reduction in Hair Fall (Instant Hair Loss Control) 2. Improvement in Visible Hair Growth and Follicular Density 3. Overall Hair Quality Composite Score 4. Investigator Global Assessment (IGA) Hair Thickness and StrengthTimepoint: Day 0 (Baseline), Day 1 to7, Day 14, Day 30 ( 3), Day 60 ( 5), Day 90 ( 5), Day 120 (End of Study) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Improvement in hair texture, smoothness, shine, and manageability 2. Hair breakage reduction and enhanced shaft strength 3. Visible hair growth and density improvement 4. Early control of hair fall 5. Aesthetic improvement in hair appearance 6. Investigator Global Assessment (IGA) 7. Subjective scalp comfort and user satisfactionTimepoint: Day 0 (Baseline), Day 1 to7, Day 14, Day 30 ( 3), Day 60 ( 5), Day 90 ( 5), Day 120 (End of Study) | — |
Countries
India
Contacts
Pankajakasthuri Ayurveda Medical college and PG centre