A Comparative, Single Center, Randomized, Double-blinded, Parallel, Placebo-controlled Study to Evaluate the Efficacy of Nabilone (Cesamet) as Adjunctive Therapy to Gabapentin (Neurontin) in the Management of Neuropathic Pain (NPP) Symptoms in Subjects With Multiple Sclerosis (MS)
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- VAS
研究概览
简要总结
The purpose of this study is to determine whether nabilone (Cesamet) when used as an adjunctive agent with gabapentin (Neurontin) provides significantly improved pain relief over gabapentin alone for the management of neuropathic pain in MS.
详细描述
Neuropathic pain syndromes, which occur due to damage to central and/or peripheral nerve axons, are often more difficult to manage and are commonly refractory to the conventional analgesia approach described by the World Health Organization, including NSAIDs and narcotic agents. These pain syndromes are often described by symptoms of burning, stabbing, crawling, shock-like, numbness and/or tingling, and can be quite concerning to the patient, especially when there is an inadequate response to treatment. It has been estimated that the prevalence of chronic pain in MS ranges anywhere from 30-90%, placing it as the second worst disease-induced symptom experienced by this patient population.
The pathophysiologic causes of this pain syndrome are complex and multifaceted, with no one specific link attributed to the pain response. Due to the complexity of neuropathic pain - which is only partially understood at best - it may be necessary in many cases to treat the source of the pain with more than one agent in order to address the many different contributors to this pain process. More thorough review of how the currently available agents for NPP work together would provide clinicians with safety and efficacy data which would aid in providing optimal pain management.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males and females between the ages of 18-65 years old with clinically definite RRMS
- •EDSS of < 6.5
- •Current treatment with gabapentin that is not effective at a stabilized dose of (>1800mg/day) for at least 1 month.
- •Visual Analogue Scale score for NPP symptoms > 5; pain present for at least 3 months
- •Negative serum pregnancy test for all females of childbearing age; not currently breastfeeding
- •No history of alcohol or substance abuse
- •No history of non-psychotic emotional disorders
- •No significant hepatic or renal insufficiency
- •No significant cardiovascular disease or hypertension
- •No known hypersensitivity and/or allergy to nabilone or its derivatives
- •No current use of cannabinoid or related products
排除标准
- 未提供
研究组 & 干预措施
Active
干预措施: nabilone (Drug)
placebo
干预措施: placebo (Other)
结局指标
主要结局
VAS
时间窗: 9 weeks
次要结局
- PGIC(9 weeks)
- SF MPQ(9 weeks)
- SF-36(9 weeks)
