TCTR20210923001已完成不适用
Prospective study and cost-effectiveness analysis of the outcomes of advanced pain interventions in Thailand)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 7 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •1) The patients were more than 7 years old
- •2) The patients suffered from chronic intractable pain from FBSS, PVD or neuropathic pain
- •3) The patients reported no satisfactory response to previous treatment defined by a pain score (numeric rating scale or NRS) of at least 5 out of 10 for at least 2 years, despite physical therapy, appropriate regimen of pain medication (gabapentin dose of more than 900 mg/day or pregabalin more than 150 mg/day and two or more other pain medications), other pain interventions or surgery.
- •SCS+CMM group
- •Any patients who underwent a successful SCS trial and subsequent implantation.
排除标准
- •1. Refusal to participate in the study
- •2. Pain due to cancer 3. Difficulty of communication or poor literacy of Thai language
研究者
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