CTRI/2022/07/044250进行中(未招募)3 期
An Open Label, Prospective, Non-Randomised, Non-Comparative, Single Arm Clinical Study to Evaluate the Effectiveness, Safety and Tolerability of â??Essen Merry Glowâ?? of Essen Fooddies India Pvt. Ltd as a Collagen Drink for Skin, Hair and Nail Health in Adults.
Essen Fooddies India Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 进行中(未招募)
- 发起方
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
入选标准
- •1.Clinically healthy adults, between the ages of 30 and 65 years (both ages and all genders inclusive) looking to improve their skin, nail and hair health.
- •2.Subjects with any skin type who along with fine lines and wrinkles must have any one of the following concerns.
- •ii.Dull Hair
- •iii.Brittle and Thin Hair including hair breakage
- •iv.Brittle Nails
- •3.Subjects who are willing to abstain from use of herbal, allopathic or other nutritional supplements that are indicated at improving skin, hair and nail health.
- •4.Subjects who are willing to give informed consent for participation, able to comprehend and understand the responsibilities during screening and treatment period.
- •5.Subjects who are willing not to participate in any other clinical trial during participation in the current trial.
排除标准
- •1.Subjects with known hypersensitivity or ethical objection to the ingredients of the investigational product
- •2.Subjects who have no dermatological condition of the skin, nail or hair that impedes with basic physical examination or determination of efficacy of investigational product on the skin.
- •3.Subjects who on active treatment for skin, hair and/or nail conditions
- •4.Subjects who have nail biting habit.
- •5.Subjects on remission from cancer of any type less than 5 years at the time of screening
- •6.Subjects who are planning a pregnancy and/or currently breastfeeding.
- •7.Subjects who have participated in a clinical study less than 1 month before screening.
- •8.Any significant medical condition (e.g., significant psychiatric or neurological disorders, active alcohol/drug abuse, etc.), any medical condition that is unstable/poorly controlled or other factor (e.g., planned relocation) that the Investigator felt would interfere with study evaluations and study participation.
- •9.Subjects who mentally unable to comprehend the responsibilities and adhere to the stipulations of the protocol.
- •10.Subjects, who in the opinion of the Investigator are not eligible for enrolment in the study.
研究者
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