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Evaluation of safety & Efficacy of skin care formulation

Completed
Conditions
The subjects selected for this study are healthy females aged between 35 and 55 years, having crows feet wrinkles & fine lines, visibly loose skin
Registration Number
CTRI/2022/05/042503
Lead Sponsor
Transformative Learning Solution Pvt Ltd
Brief Summary

The objectiveof this study will be to evaluate the safety and efficacy of a skin careformulation in terms of reduction in appearance of wrinkles & fine lines &visible improvement in skin firmness, skin moisturization, skin plumpness &skin smoothness on healthy female subjects

Product : YAUVARI  AMPLIFIED YOUTH-SPRING (0321) : Product A

The evaluationis performed using : Subject’s Self Evaluation, DermatologicalEvaluation: Safety, Dermatological Evaluation: Efficacy, Cutometry (R0parameter for skin firmness), Corneometry (Capacitance parameter SkinMoisturization), Illustrative Images of the whole face & ¾ th face underdiffuse light

Total durationof the study: 28 days following the first application of product.

Kinetics: T0, T+8 hours after productapplication, T+7 days, T+14 days and T+28 days

Productapplication : Twice a day application on whole face for the period of 28days

Number ofvolunteers: 33 + 3 female subjects

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
36
Inclusion Criteria

1)Indian Female subjects 2)Healthy subjects (no infectious and evolutive pathology which could make the subject vulnerable and stop the study, no pathology which could interfere with the study, no symptom in the process of an exploratory checkup) 3)Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar) 4)Having crows feet wrinkles, fine lines & visibly loose skin.

Exclusion Criteria
  • 1Female subjects who are pregnant (determined by Urine pregnancy test) or breastfeeding or having stopped to breastfeed in the past three months 2Having refused to give her assent by not signing the consent form 3Taking part in another study liable to interfere with this study 4Being insulin-dependent diabetic or non insulin-dependent diabetic with a recent therapy (less than 6 months) 5Having a progressive asthma (either under treatment or last fit in the last 2 years) 6Being epileptic.
  • 7Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months) 8Having cutaneous hypersensitivity 9Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.
  • 10Having known allergy to any of the Ingredient of the Test Product 11Following 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) 12Having consumed caffeine-based products (coffee, cola, tea …), alcohol, highly spiced foods and/or smoked in the two hours preceding the measurements 13Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months.
  • 14Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit 15Having applied a cosmetic product (included make-up) or skin care product on the studied areas on the day of the study (only face cleaned with water is accepted) 16Refusing to follow the restrictions below during the study:Do not take part in any family planning activities leading to pregnancy and breastfeeding, Do not take part in another study liable to interfere with this study, Do not take 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), Do not consume any caffeine-based products (coffee, cola, tea …), alcohol, highly spiced foods and/or smoked in the two hours preceding the measurements, Do not change her cosmetic habits apart from the particular conditions mentioned in the protocol, on the studied anatomic unit, During the study: Do not use other cosmetic products or skin care products other than the tested products to the studied areas.
  • (only usual cleanser/soap is accepted), The day of the measurements : No test product must be used (only test site cleaned with water is accepted) 17Having started, changed or stopped a Hormone Replacement Therapy in the past 6 months.
  • 18Having started, changed or stopped her tobacco consumption (for smokers consuming more than 10 cigarettes per day) in the previous 6 months.
  • 19Having taken a Dehydroepiandrosterone based treatment in the previous 6 months.
  • 20Having applied products with an anti-wrinkle action particularly firming products (Retinoic acid, retinol, retinaldehyde, Alpha Hydroxy Acid….) in the 2 weeks preceding the start of the study.
  • 21Having made injections of anti-wrinkle products (collagen, hyaluronic acid, botulinic toxin…) in the previous 12 months.
  • 22Having undergone techniques with aesthetic aim (chemical peel, mechanical dermabrasion, laser, pulsed flash lamp …) in the previous year.
  • 23Having undergone surgery of the skin-muscular slackening on the face (lifting) in the previous 5 years.
  • 24Taking oral supplements with major or minor effect on whitening of skin (e.g. vitamin C, beta-carotene…) 25Having applied products with a depigmenting action (hydroquinone or derivates…) in the 4 weeks preceding the start of the study.
  • 26Having undergone physical and/or chemical treatments of the spots (liquid nitrogen, dry ice, pulsed flash lamp, dermabrasion, chemical peel …) in the previous 6 months.
  • 27Having a suntanned skin on the studied areas which could interfere with the evaluations of the study.
  • 29Having practiced sport, the day of start of the study.
  • 31Refusing to follow the restrictions below during the study: Do not start, change or stop a hormonal treatment (hormonal contraception, Hormone Replacement Therapy),Do not start a medicinal treatment which could lead to hyper pigmentation, Do not use products or techniques or surgery with an anti-wrinkles/ anti ageing action /firming action and depigmenting/ whitening action, Do not start an oral or local retinoid-based treatment, Do not have beauty treatment (e.g. skin cleansing, exfoliation, scrub, mask …) or apply self-tanning products, Do not practice water activities (swimming pool, sauna, hammam, balneotherapy.), Do not practice sport the days of study, Do not expose herself to the sun by respecting a strict photo-protection.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
safety, reduction in appearance of wrinkles & fine lines & visible improvement in skin firmness, skin moisturization, skin plumpness & skin smoothnessbaseline, 8 hours after product application, 7 days, 14 days,28 days
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mascot Spincontrol India Pvt. Ltd.

🇮🇳

Mumbai, MAHARASHTRA, India

Mascot Spincontrol India Pvt. Ltd.
🇮🇳Mumbai, MAHARASHTRA, India
Dr Raji Patil
Principal investigator
02243349191
raji@mascotspincontrol.in

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