NCT05687929招募中不适用
Real-World Registry Study on Clinical Analgesic Effect of Acetylaconitine Tablets
Ke Ma1 个研究点 分布在 1 个国家目标入组 3,500 人开始时间: 2023年3月27日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 3,500
- 试验地点
- 1
- 主要终点
- VAS (0-100mm), IDpain
研究概览
简要总结
- To observe the clinical analgesic effect, safety and adverse reactions of acetylaconitine.
- To study and analyze the main influencing factors of the acetylaconitine tablets.
详细描述
The outpatients/inpatients meeting the criteria are included into this study after signing the Informed Consent Form. The patients received 5 visits in total, which take place after the patients are included into the real-world study, on the 3rd day after enrollment and at the 1st, 4th, 8th and 12th weeks thereafter, in the form of outpatient follow-up, telephone follow-up and APP follow-up.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with chronic pain > 1 month and VAS > 40 mm Patients who can take the acetylaconitine tablets orally
排除标准
- •Patients who cannot communicate or receive follow-up Patients allergic to acetylaconitine Patients who have taken the acetylaconitine drugs orally
结局指标
主要结局
VAS (0-100mm), IDpain
时间窗: December 2022 to December 2023
Pain score
次要结局
未报告次要终点
研究者
Ke Ma
Principal Investigator
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
研究点 (1)
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