Evaluation of the Role of the Noradrenergic System in Pain Perception in Parkinson's Disease
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 28
- 试验地点
- 1
- 主要终点
- Subjective pain threshold determined using thermal stimulations (thermotest) with the method of levels
研究概览
简要总结
Patients suffering from Parkinson's disease (PD) frequently experienced painful sensations that could be, in part, due to a central modification of nociception mechanisms. Previous studies have shown that pain perception was altered in Parkinson's disease (subjective and objective pain thresholds and pain-induced cerebral activity) and that administration of L-Dopa normalized this alteration. In the central nervous system, L-Dopa is converted in dopamine and in norepinephrine. Apomorphine (a dopamine agonist) has no effect on pain threshold and pain-induced cerebral activity. Therefore the noradrenergic system could be involved in pain alteration in PD.
To assess the role of noradrenergic system in pain in patients with PD, we chose duloxetine (norepinephrine and serotonin reuptake inhibitor)because a recent study had shown that duloxetine allowed an improvement of pain clinical scores (pain questionnaires) in patients with PD.
36 patients will be enrolled in this study. We supposed that a chronic intake of duloxetine increase the pain perception level compare to the placebo. This increase would be the same than those observed with L-Dopa.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 30 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with clinical diagnosis of Parkinson's disease according to the criteria of the UKPDSBB
- •Parkinson's disease patients with a score ≤ 3 on the Hoehn and Yahr scale
- •Patients treated with dopaminergic antiparkinsonian drugs (L-Dopa, dopamine agonists, ICOMT...)
- •Patients affiliated to a social protection program
- •Women with efficacy contraception
排除标准
- •Patients suffering from another pathology causing chronic pain (rheumatic disease, traumatic or orthopedic pathologies...)
- •Parkinson's disease patients with a score > 3 on the Hoehn and Yahr scale
- •Depressed patients (MADRS score < 16)
- •Patients suffering from a cancer
- •Patients under tutelage, curatella or law protection
- •Patients with a complete contraindication against apomorphine injections or duloxetine administration (selective serotonin reuptake inhibitor and monoamine oxydase inhibitors)
- •Patients without any control of their arterial hypertension
- •Patients with a neuroleptic treatment
- •Pregnant women
研究组 & 干预措施
duloxetine
The first group (12 patients) will receive, after 28 days of duloxetine treatment, one duloxetine dose, an injection of apomorphine and a placebo of L-Dopa.
干预措施: duloxetine (Drug)
duloxetine
The first group (12 patients) will receive, after 28 days of duloxetine treatment, one duloxetine dose, an injection of apomorphine and a placebo of L-Dopa.
干预措施: injection of apomorphine (Drug)
duloxetine
The first group (12 patients) will receive, after 28 days of duloxetine treatment, one duloxetine dose, an injection of apomorphine and a placebo of L-Dopa.
干预措施: injection of placebo of L-Dopa (Drug)
positive control (L-Dopa)
The second group (12 patients) will receive, after 28 days of placebo treatment, one placebo dose of duloxetine, an injection of apomorphine and injection of placebo of L-Dopa.
干预措施: placebo of duloxetine (Drug)
positive control (L-Dopa)
The second group (12 patients) will receive, after 28 days of placebo treatment, one placebo dose of duloxetine, an injection of apomorphine and injection of placebo of L-Dopa.
干预措施: injection of apomorphine (Drug)
positive control (L-Dopa)
The second group (12 patients) will receive, after 28 days of placebo treatment, one placebo dose of duloxetine, an injection of apomorphine and injection of placebo of L-Dopa.
干预措施: injection of placebo of L-Dopa (Drug)
negative control
The third group will receive, after 28 days of placebo treatment, one placebo of duloxetine, an injection of placebo of apomorphine and a dose of L-Dopa.
干预措施: placebo of duloxetine (Drug)
negative control
The third group will receive, after 28 days of placebo treatment, one placebo of duloxetine, an injection of placebo of apomorphine and a dose of L-Dopa.
干预措施: injection of placebo of apomorphine (Drug)
negative control
The third group will receive, after 28 days of placebo treatment, one placebo of duloxetine, an injection of placebo of apomorphine and a dose of L-Dopa.
干预措施: L-Dopa (Drug)
结局指标
主要结局
Subjective pain threshold determined using thermal stimulations (thermotest) with the method of levels
时间窗: One month
Before duloxetine intake and after one month of chronic duloxetine intake
次要结局
- Clinical evaluation of the severity of the motor handicap of patients using the Unified Parkinson's Disease Rating Scale (UPDRS III)(One month)
- Objective pain threshold determined recording the nociceptive reflex of flexion(One month)