NCT00245401已完成4 期
CYPHERTM Stent Post-Marketing Surveillance Registry (US-PMS)
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 2,070
- 主要终点
- MACE at 30 days, 6 months and 1 year.
研究概览
简要总结
The purpose of this PMS registry, named e-CYPHER Stent Registry, is to collect post marketing surveillance data on the CYPHERTM Sirolimus-eluting Coronary Stent following marketing approval, when used in normal clinical practice within the labeled indications.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Cypher stent
排除标准
- 未提供
结局指标
主要结局
MACE at 30 days, 6 months and 1 year.
次要结局
- There is no pre-specified secondary outcome.
研究者
相似试验
已完成
不适用
The VIRTUE Post Marketing Surveillance RegistryAortic DissectionNCT01213589Medtronic Endovascular100
终止
不适用
Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data CollectionCerebral AneurysmNCT02281721Stryker Neurovascular150
已完成
不适用
e-BioMatrix PostMarket Surveillance RegistryCoronary Artery DiseaseNCT01254487Biosensors Europe SA1,121
Unknown
不适用
Medigus Ultrasonic Surgical Endostapler (MUSE) RegistryGastroesophageal Reflux Disease (GERD)NCT02366169Medigus Ltd200
招募中
不适用
Serranator POINT FORCE RegistryPeripheral Artery Disease (PAD)Dysfunctional AV FistulaDysfunctional AV GraftNCT06687590Cagent Vascular LLC500