ISRCTN09524995已完成未知
A randomised, double-blind, cross-over, placebo controlled clinical trial to demonstrate the proof of concept for a product designed to protect against development of head louse infestation
Thornton & Ross Ltd (UK)0 个研究点目标入组 68 人开始时间: 2012年10月19日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 68
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
- 性别
- All
入选标准
- •1. Both males and females attending school with no upper age limit, although they must be the youngest qualifying member of the household
- •2. People who are confirmed to be at risk of infestation with head lice
- •3. People who give written informed consent, or if the participant is under 16 years of age whose parent/guardian gives written informed consent to participate in the study
- •4. People who will be available for home visits by study team members over the 14 weeks of the study
排除标准
- •1. People with a known sensitivity to any of the ingredients in Octanediol 1% Solution, Hedrin Once liquid gel or the placebo leave in conditioner preparation
- •2. People with a secondary bacterial infection of the scalp (e.g. impetigo) or who have a long term scalp condition (e.g. psoriasis of the scalp)
- •3. Pregnant or nursing mothers
- •4. People who have participated in another clinical study within 1 month before entry to this study
- •5. People who have already participated in this clinical study
研究者
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