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Effect of Products on dandruff

Evaluation and comparison of in-vivo safety and efficacy of two hair care formulations in terms of Anti-dandruff effect. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072014
Enrollment
72
Registered
2024-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L219- Seborrheic dermatitis, unspecified

Interventions

Intervention1: Test Regime: This is a regime with 4 products in it. will be applied on the scalp and shafts. Neem Antidandruff advance antifungal Treatment, twice a week for period of 28 days.Neem Ant

Sponsors

Satiya nutraceuticals private limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Asian Indian male/female subjects. 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar.) 4.Having moderate to severe dandruff.

Exclusion criteria

Exclusion criteria: 1. for female, Being pregnant or breastfeeding or having stopped to breastfeed in the past three months 2. Having refused to give her/his assent by not signing the consent form 3. Taking part in another study liable to interfere with this study 4. Being insulin-dependent diabetic or non-insulin-dependent diabetic with a recent therapy (less than 6 months) 5. Having a progressive asthma (either under treatment or last fit in the last 2 years) 6. Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area (except for specific studies on a determined dermatosis) 7. Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months) 8. Being epileptic. 9. Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol) 10. Having cutaneous hypersensitivity. 11. Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products. 12. Having undergone a surgery requiring a general anesthetic of more than one hour in the past 6 months.

Design outcomes

Primary

MeasureTime frame
anti-dandruff effectTimepoint: Baseline, 2 days, 72 hours, Day 14, Day28

Secondary

MeasureTime frame
moisturization & sebum reductionTimepoint: Baseline, 2 days, 72 hours, Day 14, Day28

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

poojayadav@mascotspincontrol.in02243349191

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026