NCT04873089已完成不适用
RV3278AET0943 Cosmetic Product Efficacy Applied for 8 Weeks in Adults Having Oily and Acne Prone Skin: Comparative Study Versus Not Treated Group
Pierre Fabre Dermo Cosmetique1 个研究点 分布在 1 个国家目标入组 37 人开始时间: 2018年9月17日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 37
- 试验地点
- 1
- 主要终点
- Efficacy of the product on lesions count (Lucky method)
研究概览
简要总结
The aim of this study is to evaluate, at different times, the RV3278A - ET0943 cosmetic product efficacy after 8 weeks of application on the face (twice-daily application). At T1 (Baseline), T2 (4 weeks) and T3 (8 weeks), the following assessments are performed:
- The reduction of the pilosebaceous follicular ostium size in vivo (pores) on the forehead
- The clinical evaluation (count of non inflammatory and inflammatory acne lesions, IGA score) of the face
- The reduction in visible follicles
- The standardized numerical photographs of face and ¾ right and left profile in normal, parallel polarized, cross polarized and UV light
- The analysis of the skin lipids of the forehead
- The qualitative and quantitative analysis of the sebum and comedones constituents (nose wings)
This is a comparative, open-labelled study, on subjects with oily and acne prone skins on the face.
Each group includes 18 subjects.
详细描述
This study is monocentric, comparative versus non-treated group, open-labelled, exploratory, conducted in adults having oily and acne prone skin.
The study includes 4 visits for each group, including subjects' selection:
- V0: Subjects' selection
- V1: Baseline inclusion
- V2: 4 weeks, follow-up visit
- V3: 8 weeks, study end
The maximal study duration is 61 days. The front, temporal areas and nose wings are defined as the study interest areas for superficial samples.
The evaluation is at 3 times: T1 baseline, T2 at 4 weeks and T3 at 8 weeks of application of RV3278A formula ET0943 with comparison of each time versus baseline.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Other
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Criteria related to the population:
- •Male or Female aged between 18 and 35 years included
- •Subject with phototype I to IV included
- •Subject having signed his/her written informed consent for his/her participation in the study
- •Subject who is currently not participating in another clinical study
- •Subject affiliated to a social security system or health insurance, or is a beneficiary
- •For woman of childbearing potential: use of an effective method of contraception and using it during the whole duration of the study
- •Criteria related to diseases and general health:
- •Subject with oily, blemished skin and dilated pores on the face including open and closed comedones of the retention type (on the forehead, temporal areas and nose wings) and some inflammatory lesions:
- •Retention aspect: microcomedones and open comedones count on the forehead (> 10)
- •Inflammatory aspect: lesions ≤ 10 count on the whole face
排除标准
- •Criteria related to the population:
- •For woman of childbearing potential: subject pregnant or breastfeeding or planning to be pregnant during the study
- •Subject having already known allergy to latex
- •Subject having already known allergy to the test product or associated product components
- •Subject having scar(s) or other skin characteristic on the study areas (forehead, temporal areas and nose wings) and which, size is not compatible with the study realization
- •Subject who, has planned to apply exfoliating, keratolytic and/or self-tanning products on the face within 2 weeks prior to inclusion.
- •Subject who, has planned to be exposed to the natural or artificial UV during the study
- •Subject who is not likely to be compliant with study-related requirements
- •Subject deprived of freedom by administrative or legal decision or under guardianship
- •Criteria related to diseases and general health:
- •Inflammatory or immunological dermatosis (atopic dermatitis, psoriasis, severe inflammatory acne, cutaneous seborrhoeic dermatitis, vitiligo of the face..) of the face, or other dermatological face illness in progress at the time of inclusion on the sample areas (pigmentation of the sample areas by melasma, solar erythema or artificial post UV...)
- •Criteria related to treatments
- •Facial treatments :
- •Any topical anti-acne antibiotics (topical Erythromycin or topical Dalacin) applied during more than 5 consecutive days within 4 weeks before the inclusion
- •Any topical treatment (dermo corticoids, retinoids, antibiotics, antifungals...) ongoing or applied within 4 weeks before the inclusion
- •Oral intake of antibiotic, zinc gluconate or hormonal anti-acne treatments, ongoing or taken during more than 5 consecutive days within the month before the inclusion
- •Oral intake of isotretinoin within 6 months before the inclusion
- •Anti-inflammatory treatments (steroids or no steroids) according to the investigator's assessment
- •Hormonal contraception established or modified within 3 months before the inclusion
- •Application of skin care product containing exfoliating, keratolytic or self-tanning ingredients applied on the face within 15 days before the inclusion
- •Oral treatment (cardiovascular, endocrinal, rheumatological, urogenital, neuropsychiatric, immunosuppressant) established within 2 months before the inclusion not stabilized
- •Hygiene, skin care or make-up habits modified within less than one month before the inclusion
结局指标
主要结局
Efficacy of the product on lesions count (Lucky method)
时间窗: Change from baseline to 8 weeks later, for each group
Inflammatory and lesions quantification on the whole face
次要结局
- Skin lipids(Change from baseline to 4 weeks and 8 weeks later, for each group, on the target area)
- Pilosebaceous follicular ostium size in vivo(Change from baseline to 4 weeks and 8 weeks later, for each group, on the target area)
- Visible follicles quantification by in vivo visualisation methods(Change from baseline to 4 weeks and 8 weeks later, for each group, on the target area)
- Investigator Global Assessment (IGA) on 5-point scale(Change from 4 weeks to 8 weeks later, for each group, on the target area)
- Comedones lipid harvest and analysis(At baseline and after one month of tested product treatment)
- Forehead acne lesions count (target area)(Change from baseline to 4 weeks and 8 weeks later for each group, on the target area)
- Sebum harvest and analysis(At baseline and after one month of tested product treatment)
- Efficacy of the product on lesions count (Lucky method)(Change from baseline to 4 weeks later, for each group)
- Self product agreement questionnaire(At week 8, for tested group)
- Dilated pores on 5-point scale(Change from baseline to 4 weeks and 8 weeks later, for each group, on the target area)
- Patient Global Assessment (PGA) on 6-points scale(Change from 4 weeks to 8 weeks later, for each group, on the target area)
研究者
研究点 (1)
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