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临床试验/ACTRN12610000179033
ACTRN12610000179033已完成4 期

A randomised, assessor blind, parallel group comparative trial of NeutraLice Lotion, NeutraLice Advance and Banlice Mousse in the treatment of head lice in children

key Pharmaceuticals Ltd.0 个研究点目标入组 120 人开始时间: 2010年2月26日最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
5 Years 至 12 Years(—)
性别
All

入选标准

  • Male or female primary school-aged children.
  • Presence of live head lice (adults or nymphs) on the hair or scalp. The presence of live lice will be determined from a visual inspection of the hair and scalp, and dry-combing of the hair. Combing will stop immediately once live lice are detected. The presence of lice eggs alone is not a sufficient condition for inclusion in the trial.
  • Available for the duration of the trial.
  • Parent / Guardian have given written informed consent to their child’s participation in the trial.

排除标准

  • History of allergies or adverse reactions to head lice products or the components of the specific products being tested.
  • Treatment with any head lice product in the 4 weeks prior to participation in this trial.
  • Treatment with any head lice product during the trial.
  • Treatment with a head lice comb during the trial if the subject is found to be louse free on the final examination day.
  • Presence of scalp disease(s).
  • If the subject has a sibling in Grade 1-7, who lived at the same residence during the treatment period the sibling must be examined for lice and if infested, enrolled in this study or wet combed out on multiple days.
  • Subjects must have one fixed place of residence during the trial.

研究者

发起方
key Pharmaceuticals Ltd.

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