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临床试验/ISRCTN87607337
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

发起方
ROELMI HPC Srl

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