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临床试验/CTRI/2023/04/052081
CTRI/2023/04/052081已完成Unknown

A randomized, double-blinded, controlled study to evaluate the efficacy of test products in providing skin moisturization and barrier protection for up to 24 hours in healthy subjects.

Abbott India Limited0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
30

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. Healthy female subjects, as determined from a recent medical history.
  • 2. Subjects in the age group of 18-45 years (both ages inclusive).
  • 3. Subjects who present normal to dry skin on the forearm (corneometer value of 35 as maximum)
  • 4. Healthy skin in the test sites.
  • 5. Subjects willing to give voluntary written informed consent and agree to come for regular follow-up.
  • 6. Subjects willing to abide by and comply with the study protocol.
  • 7. Subjects who are willing not to participate in any other clinical study during participation in the current study.

排除标准

  • 1. Excessive hair on the test site
  • 2. A known history or present condition of an allergic response to any cosmetic products.
  • 3. Change personal nutrition habits as well as sports habits
  • 4. Start or change their oral hormonal treatment or their oral contraception
  • 5. Subject having active skin diseases (e.g., active atopic dermatitis, pigmented contact dermatitis or other cutaneous manifestations), which will interfere with the assessment.
  • 6. Subjects on oral medications (e.g. steroids, anti-oxidant) which will compromise the study.
  • 7. Subjects had cancer in the last 10 years
  • 8. Subjects with wounds, sunburn, scars, tattoos or piercings at the skin test site(s)
  • 9. Subjects with application of ointments, creams etc. for antibacterial, anti-allergic or immunosuppressive treatment of the skin at the test site(s)
  • 10. Systemic treatment which may modify the cutaneous state on the day of inclusion or in the previous 30 days, including retinoid therapy.
  • 11. History of intense sun exposure and/ photo toxicity/allergy.
  • 12. Female subjects who are pregnant, lactating or nursing.
  • 13. Chronic illness which may influence the cutaneous state.
  • 14. Subject participating in any other cosmetic or therapeutic trial.
  • 15. Any underlying uncontrolled medical illness including diabetes mellitus, hypertension, liver disease or history of alcoholism, HIV, hepatitis, or any other serious medical illness.

研究者

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