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临床试验/ISRCTN18390621
ISRCTN18390621已完成未知

Clinical assessment of a combined treatment targeting subjects with acne-prone skin

Complife Italia Srl0 个研究点目标入组 80 人开始时间: 2021年11月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
80

研究概览

简要总结

2022 Results article in https://dx.doi.org/10.7241/ourd.20223.1 (added 18/07/2022)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Good general health
  • 2. Both sexes, caucasian ethnicity
  • 3. Phototype I to IV
  • 4. Age between 18 and 50 years old
  • 5. Acne severity from 1 to 3 according to IGA, (Investigator’s Global Assessment) severity scale,
  • 6. Subjects who have not been recently involved in any other similar study
  • 7. Willingness to use for face care only the creams that will be consigned at the beginning of the study
  • 8. Willingness to submit before and after pictures
  • 9. Willingness to use during all the study period only the products to be tested
  • 10. Willingness not to use similar products that could interfere with the product to be tested
  • 11. Willingness to not vary the normal daily routine (i.e. lifestyle, physical activity, etc.)
  • 12. Subject is under effective contraception (oral/not oral); not expected to be changed during the trial
  • 13. Subject aware of the study procedures and having signed an informed consent form
  • 14. Subjects who accept not to expose in an intensive way to UV rays during the whole study duration

排除标准

  • 1. Subjects who do not meet the inclusion criteria
  • 2. Pregnant/breastfeeding female or who have planned pregnancy during the study period
  • 3. Subjects under systemically pharmacological treatment
  • 4. Subjects under locally pharmacological treatment on the skin area monitored during the test
  • 5. Subjects with congenital or acquired immunodeficiency
  • 6. Subjects under treatment with food supplements which could interfere with the functionality of the product under study
  • 7. Subjects who show other skin alterations on the monitored area
  • 8. Subjects considered as not adequate to participate in the study by the investigator
  • 9. Subjects with known or suspected sensitization to one or more test formulation ingredients
  • 10. Adult protected by law (under control or hospitalized in public or private institutions for
  • reasons other than research, or incarcerated)
  • 11. Subjects not able to communicate or cooperate with the investigator for problems related to language, mental retardation, or impaired brain function

研究者

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