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临床试验/NCT07566065
NCT07566065尚未招募不适用

Endovascular Treatment of Atherosclerotic Renal Artery Stenosis: A Prospective Randomized Controlled Study Comparing Covered Stents and Bare Metal Stents

Chinese Academy of Medical Sciences, Fuwai Hospital15 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2026年4月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
150
试验地点
15
主要终点
Change in eGFR

研究概览

简要总结

Atherosclerotic renal artery stenosis is the most common cause of secondary hypertension , increasing the risk of cardiovascular and kidney-related complications. Some small-scale studies have suggested that covered stents are effective and safe, but high-quality evidence from large-scale studies in atherosclerotic renal artery stenosis remains limited.

This study aims to evaluate whether covered stents are more effective than bare metal stents in patients with atherosclerotic renal artery stenosis. Eligible participants will be randomly assigned to receive either a covered stent or a bare metal stent. Patients will be followed for 12 months to assess Changes in eGFR, 24-hour systolic blood pressure, and 24-hour diastolic blood pressure from baseline to 12 months were compared among the groups.

The results of this study may help improve treatment strategies and guide the selection of stent type for patients with this condition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 1) Renal artery diameter stenosis ≥60%; 2) Office systolic blood pressure ≥ 160 mmHg and/or office diastolic blood pressure ≥ 100 mmHg on at least two separate days without antihypertensive medication, or office systolic blood pressure ≥ 140 mmHg and/or office diastolic blood pressure ≥ 90 mmHg while on three antihypertensive drugs at conventional doses; 3) Serum creatinine < 264 μmol/L (3.0 mg/dL); 4) Affected kidney length ≥ 7.0 cm, with residual glomerular filtration rate (GFR) ≥ 10 mL/min;

排除标准

  • 1) Unstable clinical condition rendering the patient intolerant to revascularisation therapy; 2) Urinary protein ≥2+; 3) Contrast medium allergy; 4) Renal artery anatomy unsuitable for revascularisation therapy; 5) Reference vessel diameter <3.5mm or >8mm. 6)Patients with non-atherosclerotic renal artery stenosis (such as fibromuscular dysplasia or Takayasu arteritis); 7)Reference vessel diameter < 3.5 mm or > 8 mm

研究组 & 干预措施

bare metal stents group

Active Comparator

干预措施: Bare Metal Stent (Device)

covered stents group

Experimental

干预措施: Covered Stent (Device)

结局指标

主要结局

Change in eGFR

时间窗: 12 months

Change in estimated glomerular filtration rate (eGFR) at 12 months compared with baseline

次要结局

  • Change in 24-Hour Ambulatory Systolic Blood Pressure(12 months)
  • Change in 24-Hour Ambulatory Diastolic Blood Pressure(12 months)
  • Change in Office Systolic Blood Pressure(12 months)
  • Change in Office Diastolic Blood Pressure(12 months)
  • Change in Home Systolic Blood Pressure(12 months)
  • Change in Home Diastolic Blood Pressure(12 months)
  • Change in antihypertensive medication burden(12 months)
  • Stent patency(12 months)
  • Incidence of perioperative complications(1 month)
  • MACE(12 months)
  • Renal Adverse Events(12 months)

研究者

发起方
Chinese Academy of Medical Sciences, Fuwai Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiongjing Jiang

Chief Physician, Department of Cardiology

Chinese Academy of Medical Sciences, Fuwai Hospital

研究点 (15)

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