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临床试验/CTRI/2023/07/054901
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

发起方
Adret Retail Pvt. Ltd. (Kapiva Ayurveda)

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