IVIG for Treatment of Resistant Neuropathic Pain: a Preliminary Study
试验速览
- 阶段
- 2 期
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- The primary outcome measure will consist of change in mean daily pain diary score from baseline to each week post-treatment
研究概览
简要总结
This project addresses a vexing problem that has alluded the best efforts of the medical/scientific community: treatment of resistant neuropathic pain. Neuropathic pain is common and includes conditions such as diabetic neuropathy, post herpetic neuralgia and post stroke pain and is believed to affect at least 3% of adults. Surveys of patients with neuropathic pain indicate that 60% do not receive adequate relief with current treatment. Results from recent laboratory and human studies reveal a new approach to treatment. This approach is based on the findings that neuroinflammation appears to be involved in development and maintenance of neuropathic pain. This study explores the effects of an immune-modulating blood-derived product, intravenous immunoglobulin (IVIG), in treating neuropathic pain. IVIG is thought to reduce neuroinflammation contributing to neuropathic pain. If successful, the study will provide important insights into pain mechanisms and a better understanding of how IVIG relieves neuropathic pain.
Hypotheses:
- Reduction in neuroinflammation (NI) markers will co-vary with clinical indicators of pain relief
- Patients with higher levels of markers of NI will be more likely to respond to IVIG
详细描述
This study will employ a randomized double blind cross-over design. A total of 12 subjects will be recruited for the study. Once each subject has satisfied the inclusion and exclusion criteria and provided informed consent, the subject will be randomized to either the IVIG or placebo treatment groups, using a pre-determined randomization list generated by the research office at the University of Calgary. Complete responders will begin a monitoring phase, partial and non-responders will return for a second cycle in one month. Complete responders, with prolonged relief, will cross-over to the alternative treatment when their pain returns if this occurs within 6 months of the infusion.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age >18 years; Clinical diagnosis of treatment-resistant neuropathic pain;
- •Score of 4/10 or greater on the DN4 NeP screening questionnaire;
- •Bedside examination confirming symptoms of neuropathic pain;
- •Moderate to severe pain;
- •Completed adequate analgesic trials according to neuropathic pain clinical practice guidelines;
- •provides informed consent
排除标准
- •Pregnant or lactating women;
- •Clinical diagnosis of phantom limb pain;
- •History of psychosis;
- •current, substance dependency disorder;
- •presence of clinically significant cardiac or pulmonary disorder that would compromise participants' safety;
- •severe pain disorder other than the chronic NeP under study;
- •Abnormalities above 1.5 times upper range of normal on screening CBC, blood chemistry;
- •Serum IgA less than <0.05 g/L
结局指标
主要结局
The primary outcome measure will consist of change in mean daily pain diary score from baseline to each week post-treatment
时间窗: Performed at screening, before the initial infusion, 2 weeks and 4 weeks post treatment
次要结局
- Measurement of neuroinflammation (NI) markers (IL-1β, IL-6, IL-8, TNF-α, MMP-9, TIMP-1)(Performed at screening, before the initial infusion, 2 weeks and 4 weeks post treatment)