CTRI/2021/10/037046已完成未知
Placebo controlled clinical trial to assess the efficacy and safety of (GOOD NIGHT) after-bite roll-on in reducing mosquito bite induced erythema in Paediatric and adult population
Godrej Consumer Products Pvt Ltd India0 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
- 未知
- 状态
- 已完成
- 发起方
- 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
- •Participants of either sex aged more than 3 months of age.
- •Participants/parents/guardians who are able to comply with all study requirements with a willingness to participate and give written informed consent(parent/guardian) voluntarily.
- •Participants with at least 2 mosquito bites in any part of the arm, leg or face.
- •Familiarity with an immediate mosquito bite reaction.
- •History of immediately responding to mosquito bites with itching.
- •Willing and able to refrain from consuming anti-histamines, corticosteroids, or Non- Steroid Anti-Inflammatory Drugs (NSAID,) for a time period of 1 week prior to the beginning of the study, and continuing throughout the course of the study.
- •Willing to abstain from the use of insect repellant and/or any treatment other than the test device for the relief of mosquito bite symptoms until after the study
排除标准
- •Known allergy to compounds of investigational product.
- •No history of prior affliction with mosquito bites.
- •History of lack of reaction to mosquito and/or other insect bites that includes itching.
- •Current use of steroids.
- •Use of insect repellants during the week prior to study start.
- •Presence of any cardio vascular co morbid conditions.
- •Epilepsy or other neurological disorders.
- •Severe case of itching or erythema.
- •Any skin or other disease or illness that can cause or influence skin itching, such as Psoriasis.
- •Participation in research over the preceding 90 days.
研究者
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