CTRI/2022/12/047967已完成未知
An open label clinical study to evaluate the Safety, Tolerability andIn-use efficacy of HBWW-052005
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 84
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 subjects in the age group as below (inclusive of both genders).
- •Group 1: >=18-<=45 years (both inclusive).
- •Group 2: >= 2 - -<=12 years (both inclusive).
- •Group 3: 0 months â?? -<=2 years (both inclusive).
- •Group 4: Premature babies (babies born before 37 weeks).
- •2.Healthy day 1 babies not requiring medical attention.
- •3.Babies with signs of atopic dermatitis (dry skin, itchy skin, redness, sensitive skin, rashes) who does not require medical/ systemic treatment to be included. Included in group 2 (6 subjects) and group 3 (15 subjects) with signs of atopic dermatitis.
- •4.Subjects in general good health as determined from a recent medical history.
- •5.Subjects mother/legal representative, preferably mother willing to give a voluntary written informed consent and agree to come for regular follow up.
- •6.Subjects mother/legal representative, preferably mother willing to abide by and comply with the study protocol.
- •7.Subjects should not participate in any other clinical study during participation in the current study.
排除标准
- •A known history or present condition of allergic response to any
- •other concern that may require medical attention.
- •Chronic illness which may influence the cutaneous state.
- •Subjects not willing to stop the use of other baby powders
- •during the study period.
- •Subjects participated in any other clinical study past 4 weeks
研究者
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