EUCTR2012-000839-54-DK进行中（未招募）不适用
The effect of late naloxon-infusion on secondary hyperalgesia after a first degree burn injury
相关药物
试验速览
- 阶段
- 不适用
- 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
- •Age betwen 20 and 35
- •Volunteers that have given there written concent to participate in the clinical trial and understand the trial.
- •Urinary test with no trace of opioids
- •Negative pregnancy test
- •Body mass index (BMI): 18 < BMI < 30
- •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 22
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Volunteers that can not cooperate
- •Volunteers that do not understand and read danish
- •Women who are planning to be pregnant, are pregnant or are breastfeeding
- •Women how do not use birthcontrol
- •Have been in another clinical trial the last 60 days
- •Any form of injury or any other influence of the nerves on the calf
- •Any neurological disease
- •use of any psychoactive drugs
- •Abuse of alcohol or drug
- •Chronical pain
- •regular use of analgesia (more than twice a week)
- •Know allergy to morphine or other morphine drug incl. Naloxon
- •Skin lesion on the calf
- •Has taken medicin prescription a week before the trial
- •Has taken over the counter medicin 48 hours before the trial
- •Psychological instabel - investigators evaluation
研究者
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