Status:
COMPLETED
A Randomized, Double-blinded, Placebo Controlled, Monocentric Study to Evaluate the Anti-ageing and Skin Brightening Benefit of the Test Product in Healthy Female Subjects
Lead Sponsor:
Ratan K. Chaudhuri
Conditions:
Skin Aging
Eligibility:
FEMALE
35-50 years
Phase:
NA
Brief Summary
Every day the cells of the outer layer of skin die off, shed, and regenerate. When young, skin cells turn over quickly, but that turnover rate begins to slow with age, beginning as early as twenties. ...
Detailed Description
Every day the cells of the outer layer of skin die off, shed, and regenerate. When young, skin cells turn over quickly, but that turnover rate begins to slow with age, beginning as early as twenties. ...
Eligibility Criteria
Inclusion
- Female adult subjects in general good health as determined from a recent medical history, general physical examination, dermatological assessment.
- Subjects in the age group of 35-50 years (both ages inclusive).
- Subject with Fitzpatrick skin types III to V (ITA to be recorded at forehead and flexor forearm)
- Subjects with chronic pollution exposure in past 5 years based on pollution questionnaire (Refer annexure 1)
- Subjects with normal to dry skin type (corneometer reading upto 35)
- Subjects with mild to moderate fine lines and wrinkles in periorbital area (Crow's feet-under eye) \& forehead (Refer annexure 3 for photonumerical scale)
- Subjects with minimum one spot with width ≥3 mm
- Subjects with chronic pollution exposure in past 5 years based on pollution questionnaire (Refer annexure 1)
- Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face.
- Subject who agrees not to use any other product/treatment/home remedy/ except the provided product on their face during the study period other than the test product.
- Subjects who agree not to carry out bleaching or any other procedures including facial etc. on face during the study period.
- Subjects who agree not to expose to excessive sun light. (Sun exposure not more than half an hour daily and during that time use of umbrella to cover face).
- Subjects willing to give a voluntary written informed consent, photography release and agree to come for regular follow-up.
- Subjects willing to abide by and comply with the study protocol.
Exclusion
- Subject with any other signs of significant local irritation or skin disease.
- Subject currently taking any medication, which the Investigator believes may influence the interpretation of the data.
- Subject having clinically significant systemic or cutaneous disease, chronic illness or had major surgery in the last year.
- Subjects who do not agree to remove all jewellery on/around face (e.g., necklace, earrings, if possible nose ring), during VISIA imaging.
- Subjects having hair style which covers almost the entire forehead
- Subjects undergoing any treatment of any skin condition on their face/forearm.
- Subjects not willing to discontinue other topical facial products.
- Subject allergic or sensitive to bar cleansing products, cosmetics, creams/lotions, artificial jewellery or anything else.
- Pregnant women (as confirmed by UPT) and lactating women
- Subjects on any medical treatment either systemic/topical in the past 1 month or currently taking medication including food supplements.
- Subjects with skin allergy history or atopic dermatitis or psoriasis
- Subjects who have participated in any other clinical trial in the last 3 months.
- Subjects using oral contraceptive pills or hormonal implants as birth control measures during the study
- Subjects that was treated with Botox/filler /bio stimulatory molecules injection
Key Trial Info
Start Date :
September 3 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 30 2021
Estimated Enrollment :
26 Patients enrolled
Trial Details
Trial ID
NCT04276753
Start Date
September 3 2020
End Date
April 30 2021
Last Update
June 25 2021
Active Locations (1)
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1
MSCR
Bengaluru, Karnatka, India, 560008