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Study to check the safety and effectiveness of product on human subjects.

To evaluate the in vivo efficacy and safety of a skin care regime in terms of reduction in acne postinflammatory hyperpigmentation, improvement in skin even tone, skin brightness, hydration, Skin elasticity and skin gloss on healthy male subjects - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079217
Enrollment
72
Registered
2025-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

None listed

Interventions

Intervention1: Test Regime(Brightening pro cleanser+Brightening pro serum+Brightening pro sunscreen SPF 50+ PA++++): Products of test regime are applied on the whole face for the period of 28 days. Cl

Sponsors

Anveya Living Private Limited - Haryana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Indian male subjects. 2)Healthy subjects. 3)Skin is healthy on the studied anatomic unit 4)Having normal skin type with visible Acne PIH.

Exclusion criteria

Exclusion criteria: 1. Having refused to give his assent by not signing the consent form. 2. Taking part in another study liable to interfere with this study. 3. Being insulin-dependent diabetic or non-insulin-dependent diabetic with a recent therapy (less than 6 months) 4. Having progressive asthma. 5. Being epileptic. 6. Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months) 8. Having cutaneous hypersensitivity 9. Having a diagnosed or highly probable allergy to one or several compounds of cosmetic products. 10. 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) 11. Having consumed caffeine-based products (coffee, cola, tea ), alcohol, highly spiced foods and/or smoked in the two hours preceding the measurements. 12. Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months. 13. Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit 14. Having applied a cosmetic product (included make-up) or skin care product on the studied areas the day of the study (only face cleaned with water is accepted)

Design outcomes

Primary

MeasureTime frame
Reduction in hyper-pigmentation (Acne PIH), improvement in skin even tone, skin brightness, hydration, Skin elasticity and skin glossTimepoint: Baseline, Day 7, Day 14, Day 28—

Secondary

MeasureTime frame
NilTimepoint: NA—

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