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临床试验/CTRI/2024/08/072512
CTRI/2024/08/072512已完成Unknown

A Pilot Study to Evaluate the skin lightness activity of Silphion S-33 on Healthy Human Subjects

SILPHION RESEARCH PRIVATE LIMITED,1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年8月24日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
Change in

研究概览

简要总结

Clinical study to evaluate the Skin Lightness Activity Of Silphion S-33

1. Silphion S-33

The products will be tested on 10 human volunteers.

Assessment would Notice the improvement in  Melanin content, Hydration and skin Lightness with follow-up visits on Day 0, and Day 7 with Follow up measure on 8th day.

The study is done as per BIS standard 4011

研究设计

研究类型
Observational

入排标准

年龄范围
20.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Voluntary man or women between 20 and 45 years.
  • Photo type V.
  • People with oily skin.
  • For whom the investigator considers that the compliance will be correct.
  • Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures.
  • Having signed a Consent Form.
  • Willingness to avoid intense UV exposure on test site (sun or artificial UV) during the course of the study.
  • Willingness to avoid excessive water contact (for example swimming) or activity which causes excessive sweating (that is exercise, sauna), during the course of the study.
  • Should be able to read and write (in English, Hindi or local language).
  • Having valid proof of identity and age.

排除标准

  • Pregnant or nursing mothers 2.Scars, excessive terminal hair or tattoo on the studied area 3.Dermatological infection or pathology on the level of studied area.
  • 4.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material) 5.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 6.Chronic illness which may influence the outcome of the study.
  • 7.Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month) 8.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.

结局指标

主要结局

Change in

时间窗: Day0, Day7

1. Melanin Index

时间窗: Day0, Day7

2. Lightening index

时间窗: Day0, Day7

3. Hydration

时间窗: Day0, Day7

次要结局

  • Not Applicable(Not Applicable)

研究者

发起方
SILPHION RESEARCH PRIVATE LIMITED,
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Robin Chugh

CCFT Laboratories

研究点 (1)

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