jRCT2080221311未知3 期
Long-term study of HFT-290 in patients with chronic pain.
适应症
试验速览
- 阶段
- 3 期
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 干预模型
- Multicenter, open-label, uncontrolled
入排标准
- 年龄范围
- No limit 至 No limit(—)
- 性别
- All
入选标准
- •Patients with chronic pain persisting for at least 12 weeks before obtaining informed consent
排除标准
- •Patients with abnormalities at the site of application
- •Patients in whom the primary cause of chronic pain (the target of evaluation) is considered to be persistent somatoform pain disorder
- •Patients who are scheduled to undergo an operation with a potential influence on the evaluation of pain for at least 7 days before starting administration of the investigational drug
结局指标
主要结局
-
efficacy, safety
次要结局
未报告次要终点
研究者
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