ISRCTN45553737已完成不适用
A randomised, controlled, assessor-blind, clinical trial to compare Liceko® with Nix® / Lyclear® 1% permethrin creme rinse in the treatment of head lice.
Panin S.R.L (Italy)0 个研究点目标入组 44 人开始时间: 2011年5月24日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 44
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, aged 6 months and over with no upper age limit
- •2. People who upon examination, are confirmed to have live 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 follow-up visits by study team members over the 14 days following first treatment
排除标准
- •1. People with a known sensitivity to any of the ingredients in Liceko ® or Nix® / Lyclear® 1% permethrin creme rinse, pyrethroid insecticides, or plants related to dandelions or chrysanthemums.
- •2. People with a secondary bacterial infection of the scalp (e.g. impetigo) or who have an active long-term scalp condition (e.g. psoriasis of the scalp)
- •3. People who have been treated with other head lice products within the previous two weeks
- •4. People who have bleached hair, or hair that has been permanently waved within the previous four weeks
- •5. People who have been treated with the antibiotics co-trimoxazole or trimethoprim within the previous four weeks, or who are currently taking such a course
- •6. Pregnant or nursing mothers
- •7. People who have participated in another clinical study within one month before entry to this study
- •8. People who have already participated in this clinical study
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