CTRI/2025/09/094210
Not yet recruiting
Not Applicable
to evaluate the in-vivo safety and efficacy of a facewash in terms of improvement in instant Skin brightening and Skin glow on healthy human subjects
VLCC PERSONAL CARE LTD.1 site in 1 country36 target enrollmentStarted: September 15, 2025Last updated:
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- VLCC PERSONAL CARE LTD.
- Enrollment
- 36
- Locations
- 1
- Primary Endpoint
- improvement in instant Skin brightening and Skin glow
Overview
Brief Summary
| PRIMARY OBJECTIVE:The objective of this study will beto evaluate the in-vivo safety and efficacy of a facewash in terms of improvement in instnt Skin brightening and Skin glowon healthy human subjects |
The evaluation is performed using: Subject Self Evaluation, Dermatological Evaluation: Cosmetic Acceptability, Dermatological Evaluation: Efficacy, Chromametry and Digital Photographs
POPULATION: 36 female subjects will be selected for the study.
The subjects selected for this study are healthy males aged between 18 and 65 years, having moderate oily and dull skin.
STUDY DURATION: 1 day following the first application of the product.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- Participant and Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •1.Indian female subjects 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit 4.Having moderate oily and dull skin.
Exclusion Criteria
- •Being pregnant or breastfeeding or having stopped to breastfeed in the past three months
- •Having refused to give her/his assent by not signing the consent form
- •Taking part in another study liable to interfere with this study
- •Being insulin-dependent diabetic or non-insulin-dependent diabetic with a recent therapy (less than 6 months)
- •Having a progressive asthma (either under treatment or last fit in the last 2 years)
- •Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area (except for specific studies on a determined dermatosis)
- •Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
- •Being epileptic.
- •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)
- •Having cutaneous hypersensitivity.
Outcomes
Primary Outcomes
improvement in instant Skin brightening and Skin glow
Time Frame: T0, T+15 Minutes
Secondary Outcomes
No secondary outcomes reported
Investigators
Dr Niharika Salian
MASCOT-SPINCONTROL India Pvt. Ltd.
Study Sites (1)
Loading locations...
Similar Trials
Not yet recruiting
Not Applicable
The Study to check the safety and effectiveness of product on human volunteersCTRI/2025/08/092211Baby Forest Ayurveda Private Limited66
Not yet recruiting
Not Applicable
Study to Check Safety and Effectiveness of Skin Care ProductsCTRI/2025/09/095326ClayCo. Cosmetics Pvt. Ltd.33
Not yet recruiting
Not Applicable
A study to check if the product is safe and works well on human volunteersCTRI/2025/08/092677Emami Limited66
Not yet recruiting
Not Applicable
Study to check the safety and effect of a skin care product on dark spots and skin tone.CTRI/2025/10/096541AU Naturel Beauty Pvt. Ltd (NEUDE).36
Not yet recruiting
Not Applicable
Evaluation and Comparison of 12Hour Moisturization Efficacy and Safety of a Skincare FormulationCTRI/2025/01/079508Panacea Biotec Pharma Ltd.33