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临床试验/EUCTR2006-004136-73-GB
EUCTR2006-004136-73-GB进行中(未招募)1 期

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 - Is Hedrin 4% more effective than Derbac-M for the treatment of head lice?

Thornton & Ross Limited0 个研究点开始时间: 2012年2月16日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Participants aged 6 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 MEC study team members over the 14 days following first treatment.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

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 1 month before entry to this study.
  • 8. Participants who have already participated in this clinical study.

研究者

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