Clinical trial

A Clinical Study on the Improvement of Skin and Living Conditions After Drinking Rosa Roxburghii and Pomegranate Drinks

Name
C2202112
Description
The main objective of the study is to observe changes in the subjects' skin condition and life status after 8 weeks of drinking rosa roxburghii and pomegranate drinks. This is a single-center, randomized, single-blind, controlled, 8-week (56-day) clinical study conducted in Chinese healthy women aged 25-45 years old who were offered a rosa roxburghii and pomegranate drink.
Trial arms
Trial start
2022-07-06
Estimated PCD
2022-09-02
Trial end
2022-09-02
Status
Completed
Treatment
skin care product
Subjects are uniformly using skin care products provided by the sponsor during the test. Skin care product include: WINONA sensitiveness relieving moisturizing cleansing foam, WINONA sensitiveness relieving moisturizing lotion, WINONA anti-sensitive tolerance-extreme moisturizing cream
Arms:
Blank Group, Drinks with active ingredients Rosa Roxburghii and Pomegranate
Drinks with active ingredients Rosa Roxburghii and Pomegranate
Take drinks with active ingredients such as Rosa Roxburghii and Pomegranate. Drink every morning on an empty stomach, 20ml/2 sachets/day.
Arms:
Drinks with active ingredients Rosa Roxburghii and Pomegranate
Size
70
Primary endpoint
Changes in the skin hydration
Week0(Baseline)、Week4、Week8
Changes in the skin glossiness
Week0(Baseline)、Week4、Week8
Changes in the skin firmness
Week0(Baseline)、Week4、Week8
Changes in the skin elasticity
Week0(Baseline)、Week4、Week8
Changes in the individual type angle
Week0(Baseline)、Week4、Week8
Changes in the melanin content
Week0(Baseline)、Week4、Week8
Changes in the proportion of crow's feet area
Week0(Baseline)、Week4、Week8
Changes in the proportion of fine lines under the eye
Week0(Baseline)、Week4、Week8
Changes in the CIE RGB of skin tone
Week0(Baseline)、Week4、Week8
Changes in the grade of Pigmentation
Week0(Baseline)、Week4、Week8
Skin condition Assessment after 4-week application
Week4
Skin condition Assessment after 8-week application
Week8
Eligibility criteria
Inclusion Criteria: 1. 25-45 years old, Chinese female; 2. The subject's self-reported facial problems such as dryness, roughness, dullness, and lack of elasticity; 3. The subject's BMI is between 18\~24kg/m2; 4. After the doctor's clinical evaluation, there is at least one obvious pigmentation spot with an ITA° difference of more than 10° on the face and the surrounding adjacent skin, and the diameter is not less than 3mm (it cannot be freckles, pigmented nevi, etc. that are difficult to improve clinically using topical preparations); 5. Corneometer base measurement of facial skin moisture at 15\~45 (Corneometer Unit, C.U.) Between; 6. Be in good health and free of any other chronic diseases other than skin problems or diseases being treated; 7. Voluntarily participate in the test and sign the informed consent form; 8. Willing to comply with all evaluation requirements; Exclusion Criteria: 1. Those who have used products, health foods or drugs with antioxidant and anti-aging effects in the past 2 months; 2. Those who have used any products, health foods or drugs (such as hydroquinone preparations) that affect skin color in the past 2 months; 3. Those who have used tretinoin preparations or undergone medical aesthetic treatments such as chemical peels, lasers, and pulsed light at the test site in the past 3 months; 4. Those who are inevitably exposed to long-term sunlight; 5. Intending to become pregnant, or being pregnant or breastfeeding; 6. Have a history of alcoholism; 7. Have a history of allergies; 8. Participated in any clinical trial evaluation within 1 month; 9. Those who have applied any anti-inflammatory drugs to the test site within the past two months; 10. Those who have suffered from skin diseases (such as psoriasis, eczema, psoriasis, skin cancer, etc.); 11. patients with insulin-dependent diabetes; 12. Patients with asthma or other chronic respiratory diseases who are being treated; 13. Have taken/injected anti-allergic drugs in the past 1 month; 14. Patients who have received anti-cancer chemotherapy or immunotherapy patients within the past 6 months; 15. Have a serious internal medicine disease, have any other health problems or chronic diseases; 16. Coated with retinoids, A hydroxy acids, salicylic acids, hydroquinone within the past 3 months, or prescription drugs (antibiotics, retinoids, A hydroxy acids and steroids) in use within the past 6 months, oral contraceptives (if you have been taking the same contraceptive pills for the past 6 months, you can continue to take them); 17. Experts or professionals believe that there are other iatrogenic causes that affect the results of the review.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'OTHER', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 70, 'type': 'ACTUAL'}}
Updated at
2024-02-23

1 organization

2 products

1 indication

Indication
skin_laxity
Organization
Botanee Group
Product
Skin Care