NCT00180544终止3 期
A Prospective, Non-Randomized, Multicenter, Single-Arm, Clinical Trial to Assess the Safety and Efficacy of the RX HERCULINK 14 Peripheral Stent System for Treatment in de Novo or Restenotic Renal Artery Stenosis
适应症
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 167
- 试验地点
- 2
- 主要终点
- Primary patency .
研究概览
简要总结
The purpose of this study is to evaluate the safety and effectiveness of the RX HERCULINK 14 Peripheral Stent System in treating atherosclerotic renal artery stenosis.
详细描述
A prospective, non-randomized, multi-center, single-arm clinical trial to evaluate the safety and efficacy of the RX HERCULINK™ 14 Peripheral Stent System in the treatment of suboptimal post- procedural percutaneous transluminal angioplasty (PTA) results in de novo or restenotic atherosclerotic renal artery stenoses.
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
- 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
- •Clinical diagnosis of renal artery atherosclerosis; candidate for renal artery angioplasty and stenting; blood pressure >160/90
排除标准
- •Totally occluded renal artery on the opposite side; only one functioning kidney; target lesion is in a transplanted kidney; renal insufficiency
结局指标
主要结局
Primary patency .
时间窗: at 9-months
次要结局
- Acute procedural success(Acute)
- Access site events requiring surgical repair or intervention(Acute)
- Major adverse events (e.g. death, nephrectomy, target lesion revascularization (TLR)(at 30 days)
- TLR(at 9 months)
- Renal function(measured at 1, 6, 9, and 12-month follow-up, and every three months thereafter until approximately May 2003 or until patient 169 completes 12 month follow-up.)
- Changes in blood pressure(9 months)
研究者
研究点 (2)
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