CTRI/2023/07/055135尚未招募3 期
An Open Label, Prospective, Non-Randomised, Non-Comparative, Single Arm Clinical Study the Effectiveness, Safety and Tolerability of â??FiCollaâ?? from Athos Collagen Private Limited as a Nutritional Supplement for Hair and Nail Health of Adults. - NI
Athos Collagen Private Limited0 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
- 尚未招募
- 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 adult subjects between the ages of 21 and 55 years (both ages and all genders inclusive) looking to improve their Hair and Nail Health.
- •2. Subjects who have scored greater than or equal 15 in Hair and Nail Health Screening Questionnaire.
- •3. Subjects who are willing to abstain from the use of herbal, allopathic or other nutritional supplements (interventional) that are indicated at improving 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 to the ingredients of the investigational product
- •2. Subjects who are on collagens supplements in any form.
- •3. Subjects who are vegetarians/ vegans who object to consumption of animal origin investigational product.
- •4. Subjects who had an active dermatological procedure done up to 3 months prior to screening
- •5. Subjects who have skin condition/ scarring that prevent proper examination or evaluation of study criteria.
- •6. Subjects who have an active infection, disease or disorder that will prevent them from fully satisfying the responsibilities of the study
- •7. Subjects with history of seizures, uncontrolled diabetes, hypertension or major cardiac illness like congestive heart failure etc.
- •8. Subjects on remission from cancer of any type less than 5 years at the time of screening.
- •9. Subjects who are planning a pregnancy and/or currently breastfeeding.
- •10. Subjects who have participated in a clinical study less than1 month before screening.
- •11. 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., planed relocation) that the investigator felt would interfere with study evaluations and study participation.
- •12. Subjects who mentally unable to comprehend the responsibilities and adhere to the stipulations of the protocols.
- •13. Subjects, who in the opinion of the Investigator are not eligible for enrolment in the study.
研究者
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