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Efficacy check of skin care products

To evaluate the in-vivo safety and efficacy of skin care formulation in terms of improvement in skin Moisturization, Skin Brightening, Even Skin Tone, reduction in Dark Spot and improvement Skin Radiance on healthy female subjects. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060573
Enrollment
36
Registered
2023-12-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

None listed

Interventions

Intervention1: Guava 10% Vit C Serum: Approximately 4-5 drops of test product to be applied on whole face twice a day in morning and at night for the period of 28 days. Control Intervention1: Nil: NA

Sponsors

SATIYA NUTRACEUTICALS PRIVATE LIMITED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Skin is healthy on the studied anatomic unit. 2)Having wheatish to dark complexion. 3)Having dry skin. 4)Having at least 1 Dark Spot with 3.5mm in diameter (Acne PIH).

Exclusion criteria

Exclusion criteria: 1)Having refused to give her assent by signing the consent form. 2)Taking part in another study liable to interfere with this study. 3)Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area 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)Being epileptic 7)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 the cosmetic products or food products or to latex 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 undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months. 12)Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit 13)Having applied a cosmetic product (included make-up) on the studied areas the first day of the study (only face cleaned with water is accepted).

Design outcomes

Primary

MeasureTime frame
Skin Moisturization, Skin Brightening, Even Skin Tone, reduction in Dark Spot and improvement Skin RadianceTimepoint: Baseline, 7 days, 14 days, 28 days—

Secondary

MeasureTime frame
NilTimepoint: NA—

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

raji@mascotspincontrol.in02243349191

Outcome results

None listed

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