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临床试验/NCT01851486
NCT01851486撤回不适用

The Relationships Between the Noradrenergic, Opioid and Pain System

Rambam Health Care Campus1 个研究点 分布在 1 个国家开始时间: 2013年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
The changes in pain responses after administration of alpha 2 agonist and mu receptor antagonist

研究概览

简要总结

The role of alpha2 receptor agonist on pain perception and modulation will be examined. In addition whether this is mediated through the opioid system will be examined. Pain perception and modulation will be examined before and after administration of Clonidine or placebo together with Naloxone or saline.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy volunteers
  • Age 18-40
  • No chronic disease

排除标准

  • Subjects who suffer from chronic pain / pain syndrome
  • use of anti-depressant or anti-psychotic drugs
  • suffering from cardiovascular disease
  • breast feeding

研究组 & 干预措施

Placebo +saline

Placebo Comparator

Placebo 0.15 mg+ saline 0.15 mg/kg

干预措施: placebo (Drug)

Placebo +saline

Placebo Comparator

Placebo 0.15 mg+ saline 0.15 mg/kg

干预措施: saline (Other)

Clonidine+ Saline

Active Comparator

Clonidine 0.15 mg and saline 0.15 mg/kg

干预措施: Clonidine (Drug)

Clonidine+ Saline

Active Comparator

Clonidine 0.15 mg and saline 0.15 mg/kg

干预措施: saline (Other)

Clonidine + Naloxone

Active Comparator

Clonidine 0.15 mg and Naloxone 0.15 mg/kg

干预措施: Clonidine (Drug)

Clonidine + Naloxone

Active Comparator

Clonidine 0.15 mg and Naloxone 0.15 mg/kg

干预措施: Naloxone (Drug)

Placebo +Naloxone

Active Comparator

Placebo 0.15 mg+ naloxone 0.15 mg/kg

干预措施: Naloxone (Drug)

Placebo +Naloxone

Active Comparator

Placebo 0.15 mg+ naloxone 0.15 mg/kg

干预措施: placebo (Drug)

结局指标

主要结局

The changes in pain responses after administration of alpha 2 agonist and mu receptor antagonist

时间窗: 2 years

The change in pain perception (pain thresholds and pain ratings of suprathresholds stimuli) and in the excitatory and inhibitory pain modulation responses (assessed by the temporal summation and conditioned pain modulation paradigms) will be examined before and after administration of alpha 2 agonist with and without mu receptor antagonist

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

d_yarnitsky

Professor, Head on Neurology Department

Rambam Health Care Campus

研究点 (1)

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