NCT06908538招募中不适用
Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain (VANISH)
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 2,000
- 试验地点
- 6
- 主要终点
- Primary Outcome Measure
研究概览
简要总结
The goal of this Registry is to see how the device is used when freezing nerves during an amputation procedure.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
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
- •Patients who have or will have an amputation procedure;
- •Patients who are willing and capable of providing informed consent;
- •Patients whose age is 18 years or above, or of legal age to give informed consent specific to state and national law.
排除标准
- •Women of childbearing potential who are, or plan to become, pregnant during the time of the study;
- •Other medical, social, or psychological conditions that in the opinion of the Investigator precludes the subject from appropriate consent or adherence to the protocol.
研究组 & 干预措施
Subjects who have or will have an amputation procedure.
The primary objective of this Registry is to capture real-world safety and performance data on AtriCure devices used to cryoablate nerves during an extremity amputation procedure.
干预措施: cryoablation (Device)
结局指标
主要结局
Primary Outcome Measure
时间窗: 30 days
CryoNerve Block procedural complications
次要结局
未报告次要终点
研究者
研究点 (6)
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