NCT05626504进行中(未招募)不适用
Outcome Study of the Pipeline Embolization Device With Vantage Technology in Unruptured Aneurysms
King's College Hospital NHS Trust1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年10月27日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Evaluate 30-day morbidity rates
研究概览
简要总结
In this project the investigators study the safety and efficacy of the pipeline embolization device with vantage technology in treatment of unruptured brain aneurysms
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
- •All patients treated with Pipeline Embolization Device with Vantage Technology (PEDV)
- •MRA and/or DSA (or tomographic angiography) available for follow up
排除标准
- •Insufficient background data available e.g., to determine size of aneurysm and pipeline device
- •PEDV used for causes other than aneurysms, e.g., fistulas and dissection.
结局指标
主要结局
Evaluate 30-day morbidity rates
时间窗: Done at 30 days post procedural
We will evaluate short term clinical outcome in the form of morbidity rates 30 days after the procedure
Evaluate 30-day mortality rates
时间窗: Done at 30 days post procedural
We will evaluate short term clinical outcome in the form of mortality rates 30 days after the procedure
次要结局
- Evaluate 1-year morbidity rates(Done at >30days up to 1 year post procedural)
- Evaluate 1-year mortality rates(Done at >30days up to 1 year post procedural)
研究者
研究点 (1)
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