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?
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.
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