ISRCTN47755726已完成不适用
A randomised, controlled, assessor-blind, clinical trial to demonstrate superiority of Hedrin 4% dimeticone lotion compared with Derbac-M 0.5% malathion aqueous liquid in the treatment of head lice
Thornton & Ross Ltd (UK)0 个研究点目标入组 73 人开始时间: 2006年12月27日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 73
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. Participants aged six months and over with no upper age limit
- •2. Participants who, upon examination, are confirmed to have live head lice
- •3. Participants 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. Participants who will be available for home visits by Medical Entomology Centre (MEC) study team members over the 14 days following first treatment
排除标准
- •1. Participants with a known sensitivity to any of the ingredients in Hedrin 4% lotion or Derbac-M liquid
- •2. Participants 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. Participants who have been treated with other head lice products within the previous two weeks
- •4. Participants who have bleached hair, or hair that has been colour treated or permanently waved within the previous four weeks (wash in/wash out colours are acceptable)
- •5. Participants who have been treated with the antibiotics Co-Trimoxazole, Septrin or Trimethoprim within the previous four weeks, or who are currently taking such a course
- •6. Pregnant or nursing mothers
- •7. Participants who have participated in another clinical study within one month before entry to this study
- •8. Participants who have already participated in this clinical study
研究者
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