EUCTR2004-005127-17-AT进行中（未招募）不适用
Potentiation of the antihyperalgesic effects of topically applied diclofenac by concomitant use of topical lidocaine
pharmed holding GmbH0 个研究点目标入组 10 人开始时间: 2005年4月5日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 10
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
- •Healthy volunteers of male and female sex.
- •Age 19 – 45 years.
- •BMI between 19 and 26 kg/cm2 .
- •Volunteer is healthy according to the results of the medical examination and without relevant medical problems.
- •Volunteer is able to understand and sign the Informed Consent.
- •Volunteer is able to participate in the entire study.
- •Are the trial subjects under 18? no
- •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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known sensitivity against Diclofenac or Lidocaine.
- •Participation in a study within the last 3 months.
- •Donation of blood within the last 8 weeks.
- •Use of any OTC medication within the last 3 days.
- •Use of Diclofenac or Lidocaine containing medications within the last 2 weeks.
- •Abuse of alcohol, drugs or drugs of abuse.
- •Blodd pressure (seated) lower then 90/65 or higher then 135/90 mmHg
- •Smoker, more than 20 cigarettes a day.
- •Chronic diseases in the anamnesis or acute sickness.
- •Any relevant skin disturbances or diseases.
研究者
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