NCT00301340已完成3 期
An Open Trial to Evaluate the Efficacy and Safety of Summers Non-Pesticide Lice Asphyxiator (L.A.) for the Treatment of Head Lice
Summers Laboratories10 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2006年3月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 200
- 试验地点
- 10
研究概览
简要总结
Summers Laboratories has developed a non-pesticide treatment for head lice. Lice Asphyxiator (L.A.) works by mechanically blocking the respiratory spiracles of the head lice, therefore causing a quick-acting suffocation that will not result in the development of resistance.
The objectives of this open label study are to evaluate the efficacy and safety of home use of two 10-minute treatments of 5% L.A. (applied one week apart).
研究设计
- 研究类型
- Interventional
- 主要目的
- Treatment
入排标准
- 年龄范围
- 6 Months 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males and females 6 months of age or older.
- •Have an active infestation with Pediculus capitis, the human head louse, with at least three live lice at baseline, or treatment failure with any live lice from Protocol SU-01-2005 or Protocol SU-02-
- •Agree not to use any other pediculicides or medicated hair grooming products during the duration of the study.
- •Be healthy, non-febrile, and not suffering from an infection likely to require antibiotic therapy during the study period.
- •Subject or guardian is able to understand the new HIPAA regulations and sign the HIPAA form.
- •Subject or guardian has read, understood, and signed appropriate informed consent in English. If English is not the primary language, the information about the study must be explained in their language and a copy of the informed consent must be in that language.
- •Subject is willing to participate in the study, and abide by the protocol requirements.
排除标准
- •Participation in any clinical study, excluding protocols SU-01-2005 and SU-02-2005, within the past 30 days.
- •Known hypersensitivity to any ingredient in the product formulation.
研究者
研究点 (10)
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