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临床试验/CTRI/2026/02/104260
CTRI/2026/02/104260尚未招募不适用

A clinical study to Evaluate the skin Irritation potential of Pigeon Baby Face and Body wipe on Healthy Human Volunteers

Pigeon India1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2026年3月3日

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
35
试验地点
1

研究概览

简要总结

The below product would be tested as per the guideline IS 4011:2018 and ISO 10993 Part 23 for dermal safety assessment.

  1. Baby face and body wipe

The product will be tested for skin irritation on 35 Sensitive skin volunteers.

Assessment would be done on day 0, day 1, day 2 with followup visit on day 8 for erythema and Oedema scoring.

研究设计

研究类型
Interventional
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.

研究者

发起方
Pigeon India
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Sanjay Gupta

CCFT Laboratories

研究点 (1)

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