CTRI/2023/07/054901进行中(未招募)4 期
An open label, prospective, single arm study to evaluate the Skin health enhancing ability of Kapiva Skin Foods Glow Mix- An Ayurvedic powder-based drink in healthy adult female face skin. - NI
Adret Retail Pvt. Ltd. (Kapiva Ayurveda)0 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
- 4 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. Female adult subjects in general good health & age group of 30 to 50 years.
- •2. Subject must not have used any anti-aging cream before study enrolment and intend to use during the study.
- •3. Subject who agrees not to use any other product/treatment/home
- •remedy/soap bar on their face during the study period other than the test product.
- •4. Subject with Fitzpatrick skin types III to V.
- •5. Subjects having visible fine lines and wrinkles in periorbital area like Crow’s feet-under eye & forehead as assessed by dermatologist.
- •6. Subjects having skin aging concerns as assessed by dermatologist
- •7. Subjects not having hair style which covers almost the entire forehead.
- •8. Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face.
- •9. Subjects who agree not to carry out bleaching or any other procedures on face during the study period.
- •10. Subjects who agree not to expose to excessive sun light (Sun exposure not more than half an hour daily and during that time use of umbrella to cover face).
- •11. Subjects willing to give a voluntary written informed consent, photography release and agree to come for regular follow up.
- •12. Subjects willing to abide by and comply with the study protocol.
- •13. Subjects who have not participated in a similar investigation in past four weeks.
- •14. Subjects who are willing not to participate in any other clinical study during participation in the current study.
排除标准
- •1. Subjects using any anti-aging cream prior to study enrolment and intend to use during the study.
- •2. Subject with any other signs of significant local irritation or skin disease.
- •3. Subjects who experience nausea or vomiting due to the flavor or product will be excluded from the study
- •4. Subject currently taking any medication including food supplements, which the Investigator believes may influence the interpretation of the
- •5. Subjects showing abnormal levels in blood test parameters. (Subjects having abnormal values but are clinically fit to participate in the trial
- •would be enrolled in the study at Principal Investigator’s Discretion).
- •6. Subject having chronic illness or had major surgery in the last year.
- •7. Subjects undergoing any treatment of any skin condition on their face/forearm/any.
- •8. Subjects not willing to discontinue other topical facial products.
- •9. Subjects with clinically significant cardiovascular, cerebrovascular, respiratory, liver, renal disease, congenital, or any other systemic
- •condition requiring therapeutic intervention.
- •10. A known history or present condition of an allergic response to pharmaceutical products its components or ingredients in the test products.
- •11. Pre-existing systemic disease necessitating long-term medications.
- •12. Genetic and endocrinal disorders.
- •13. Pregnant and lactating women.
研究者
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