CTRI/2024/09/073193已完成Post Marketing Surveillance
A Clinical Study to Evaluate the 48-hours Moisturization Potential of Neutriderm Multiple skin Care Formulations on Healthy Human Subjects
试验速览
- 阶段
- Post Marketing Surveillance
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Change in hydration
研究概览
简要总结
Test Product-
-
Neutriderm Moisturising Lotion
-
Neutriderm Ultimate Hydrating Cream
-
Neutriderm Foaming Cleanser
-
Neutriderm Cleansing Balm
Dose: Gently massage approx. 1 drop of Cream over one block as assigned (forearm) Route of Administration: Topical Duration: 48 hour
研究设计
- 研究类型
- Pms
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Voluntary man or women between 18 and 65 years.
- •Photo type III to V.
- •Having apparently healthy skin on test area
- •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.Henna tattoo anywhere on the body (in case of studies involving hair dyes) 4.Dermatological infection or pathology on the level of studied area 5.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye) 6.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 7.Chronic illness which may influence the outcome of the study 8.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) 9.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.
结局指标
主要结局
Change in hydration
时间窗: T0min, T+30min, T+2hrs, T+8hrs, T+24hrs, T+ 48hours
次要结局
- Change in TEWL(At t0, t24hrs and t48hrs)
研究者
Dr Robin Chugh
CCFT Laboratories
研究点 (1)
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