NCT01658787进行中(未招募)不适用
'GREAT' Global Registry for Endovascular Aortic Treatment - Outcomes Evaluation
W.L.Gore & Associates6 个研究点 分布在 4 个国家目标入组 4,600 人开始时间: 2010年12月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 4,600
- 试验地点
- 6
- 主要终点
- To collect "real world" data on the incidence of serious device events.
研究概览
简要总结
Prospective, observational Registry to obtain data on device performance and clinical outcomes.
详细描述
This is a prospective observational cohort Registry designed to obtain data on device performance and clinical outcomes of patients treated with Gore Endovascular Aortic products.
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
- •Minimum age required by state regulations
- •Indication for aortic endovascular stent graft repair
- •Signed informed consent
排除标准
- 未提供
研究组 & 干预措施
Endovascular aortic repair
Patients treated with Gore Endovascular Aortic Products.
干预措施: Endovascular aortic repair (Device)
结局指标
主要结局
To collect "real world" data on the incidence of serious device events.
时间窗: Up to 10 years
次要结局
未报告次要终点
研究者
研究点 (6)
Loading locations...
相似试验
已完成
不适用
Evaluation of the GORE® C3 Delivery System ModuleAortic Aneurysm, AbdominalNCT01398332W.L.Gore & Associates399
已完成
不适用
ROUTE Registry Of the Utilisation of the Transaortic (Tao) TAVI Approach Using the Edwards Sapien XT ValveAortic StenosisNCT01991431Institut für Pharmakologie und Präventive Medizin303
已完成
不适用
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"Critical Limb IschemiaPeripheral Arterial DiseasePeripheral Vascular DiseaseNCT02786173Metro Health, Michigan1,000
招募中
不适用
Clinical and Healthcare Outcomes From Real-World Use in the United States of a Companion AI During AF AblationAtrial FibrillationNCT06056271Volta Medical400
已完成
不适用
TOtal tRansfemoral branCHed endovasCular tHoracoabdominal Aortic Repair RegistryAortic Aneurysm, AbdominalAortic Aneurysm, ThoracicNCT04930172IRCCS San Raffaele100
