ISRCTN87607337已完成未知
Randomized, double blind, placebo controlled clinical study for evaluating the efficacy of a food supplement on cellulite-derived skin imperfections and weight control
ROELMI HPC Srl0 个研究点目标入组 60 人开始时间: 2018年7月24日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Good general health
- •3. Caucasian ethnicity
- •4. Age between 18 and 55 years old
- •5. Mild to moderate cellulite-derived skin imperfections (grade II and III of the cellulite thermographic stage)
- •6. BMI between 23 and 30.
- •7. Not been recently involved in any other similar study
- •8. Willing to follow the proposed alimentary diet for all the study time
- •9. Willing to use only the cream consigned at the beginning of the study for body care
- •10. Willing to submit to before and after pictures
- •11. Willing to use only the food supplement during the entire study period
- •12. Willing to not use products likely to interfere with the food supplement
- •13. Willing to not vary the normal daily routine (i.e. lifestyle, physical activity, etc.)
- •14. Under effective contraception (oral/not oral) that is not expected to be changed during the trial
- •15. Aware of study procedures and signed informed consent form
排除标准
- •1. Pregnant or intending to become pregnant during study
- •2. Breastfeeding
- •3. Atopy (if this interferes with the study)
- •4. Allergic to ingredients of food supplements
- •5. Allergies to cosmetic products, toiletries, sunscreens and/or topical drugs
- •6. Following anti-cellulite treatment or have followed an anti-cellulite treatment less than 3 months before the study
- •7. Used sunbeds or self-tanning product for one month before study or intend to use it during the study
- •8. Using pharmacological treatment (local or systemic) that may interfere with study
- •9. Intending to initiate any intensive sport
- •10. Other diseases that may affect outcome of study, especially metabolic or endocrine (e.g. diabetes, liver disease, kidney disorders) or any other condition that the principal investigator deems inappropriate for participation
- •11. Protected by the law (under guardianship, hospitalised in a public or private institution or incarcerated)
- •12. Unable to communicate or cooperate with the investigator
研究者
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