NCT01865591Unknown早期 1 期
A Clinical Trial for the Assessment of Safety and Efficacy of the UltraSOUND Mediated InTerVentional Treatment of Resistant Hypertension
Sound Interventions, Inc.2 个研究点 分布在 2 个国家目标入组 30 人开始时间: 2012年4月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 早期 1 期
- 发起方
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Major adverse events
研究概览
简要总结
The aim of this study is to assess the potential therapeutic benefit of catheter-based renal sympathetic denervation using therapeutic unfocussed ultrasound in a single-arm feasibility trial.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 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 85 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Uncontrolled hypertension (defined as SBP ≥ 140 mmHg during 24Hr Ambulatory BP monitoring)
- •Current treatment with ≥ 3 anti-hypertensive drugs (including at least one diuretic)
- •Renal artery diameter ≥5mm by digital angiography
- •Accessibility of renal vasculature
排除标准
- •Estimated GFR < 45
- •Type 1 Diabetes
- •Known renovascular abnormalities (eg, renal artery stenosis, previous renal artery stenting or angioplasty)
研究组 & 干预措施
Renal denervation
Experimental
Subjects are treated with unfocussed ultrasound-based renal denervation and are maintained on baseline anti-hypertensive medications.
干预措施: Ultrasound-based Renal Denervation (Device)
结局指标
主要结局
Major adverse events
时间窗: 30 days
All cause death, renal artery occlusion, renal artery stenosis, renal infarction and/or renal failure
次要结局
- Adverse events and device complications(12 months)
- Change from baseline in creatinine(6 months)
- Change from baseline in office blood pressure measurement(30 days, 3 months, 6 months, 9 months, 12 months)
- Change from baseline in ambulatory 24-hour blood pressure measurement(6 months, 12 months)
- Change from baseline in renal artery dimensions(30 days)
研究者
研究点 (2)
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