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临床试验/NCT01023373
NCT01023373Unknown4 期

Phase 4 Study of Medical Therapy Versus Medical Therapy Plus Renal Artery Stenting in Preventing the Progression of Renal Failure in Atherosclerotic Renovascular Disease

Azienda Unità Sanitaria Locale di Piacenza1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2003年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
80
试验地点
1
主要终点
Death, Initiation of dialysis therapy or either serum creatinine increase more than 20% or reduction by > 20% in estimated clearance of creatinine (with MDRD formula)

研究概览

简要总结

The aim of the study is to value, in patients with chronic kidney disease and hypertension, whether medical therapy plus interventional renal artery revascularization is superior to medical therapy alone for the treatment of hemodynamically significant (>70%) atherosclerotic renal artery stenosis, diagnosed by duplex doppler ultrasonography and confirmed by magnetic resonance angiography, in terms of avoidance of the progression of renal damage, control of hypertension and in reducing the cerebro and cardiovascular complications.

详细描述

Atherosclerotic renovascular disease (ARVD), due to renal hypoperfusion caused by mono or bilateral renal artery stenosis (RAS), is a increasing cause of chronic kidney disease and many elderly patients start dialysis due to ARDVD. Moreover ARVD is frequently progressive and reduces life-expectancy more than other causes of end stage renal disease, with a mortality rate higher than in patients with stable angina, similar to that of patients operated for colon cancer.

Unfortunately, there is not a definite therapy to cure this disease, despite important advancements in both medical therapy and in interventional radiology. Aim of the study is to see whether percutaneous transluminal interventional radiology plus stenting (PTRS) of the renal artery offers more, in terms of both preventing the progression of renal failure and controlling the hypertension, compared with the medical therapy addressed to control hypertension, improve the dyslipidemic profile and optimise the platelet anti-aggregant therapy, following the most recent guidelines. The eligible patients will be centrally randomized to:

  1. medical treatment with hypotensive drugs (all class of hypotensive agents will be used according to single-center experience including drugs agent on renin-angiotensin-aldosterone-system, when permitted), lipid lowering therapy (namely all class of statins-or hydroxymethylglutaryl-coA reductase inhibitors)and anti-platelet (acetylsalicylate and/or ticlopidine or clopidrogel according to single-center experience) or to
  2. the same medical therapy, as previously described in group a, associated with PTRS, according to a standardized protocol, with a follow up at 2 years extended to other 2 years

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
None

入排标准

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

入选标准

  • Age ≤ 80 years
  • Presence of ostial renal artery stenosis ≥ 70% (determined by Duplex Doppler ultrasonography and confirmed by Magnetic Resonance valuated by at least two experienced operators)
  • Serum creatinine ≤ 3 mg/dl and/or creatinine clearance (Modification of Diet in Renal Disease, MDRD formula)≥ 30 ml/min, defined as stage 3 or greater CKD based on National Kidney Foundation classification
  • Longitudinal ultrasonographic diameter of the stenotic kidney ≥ 8 cm
  • Blood pressure values ≤ 150/90 mmHg with the use of less than four hypotensives drugs

排除标准

  • Age > 80 years
  • Other well-known nephropathy cause of renal failure
  • Duplex doppler ultrasonography Resistive Index values >0.8
  • Total occlusion of renal artery lumen
  • Occurrence of cerebral or cardiac vascular diseases in the 6 months before the enrolment in the study
  • Malignancy with a life expectation less than one year
  • Previous documented cholesterol thrombo embolization episodes (clinically, bioptically or instrumentally)
  • Liver failure
  • Cardiac failure (NYHA IV class) or instable angina
  • Well-known intolerance or contraindications to the use of iodinated contrast media, to statins or to anti platelets drugs
  • Previous renal angioplasty
  • Pregnancy

研究组 & 干预措施

B:PTRS

Experimental

B: the same medical therapy, as previously described in group A, associated with PTRS

干预措施: PTRS (Procedure)

B:PTRS

Experimental

B: the same medical therapy, as previously described in group A, associated with PTRS

干预措施: renal artery stent (Device)

A:medical therapy

Active Comparator

hypotensive drugs, statins and antiplatelet therapy

干预措施: Medical treatment (Drug)

A:medical therapy

Active Comparator

hypotensive drugs, statins and antiplatelet therapy

干预措施: renal artery stent (Device)

结局指标

主要结局

Death, Initiation of dialysis therapy or either serum creatinine increase more than 20% or reduction by > 20% in estimated clearance of creatinine (with MDRD formula)

时间窗: 0.5, 1 and 2 years follow up plus extended 4 yrs

次要结局

  • Systolic and diastolic blood pressure values at 0.5, 1 and 2 yrs follow up, with an extended follow up after 2 yrs(0.5, 1 and 2 years follow up plus extended 4 yrs)
  • Number of hypotensive drugs(0.5, 1 and 2 years follow up plus extended 4 yrs)
  • Results of renal scintigraphy(0.5, 1 and 2 years follow up plus extended 4 yrs)
  • Incidence of complications due to interventional manoeuvres(0.5, 1 and 2 years follow up plus extended 4 yrs)
  • Changes in the incidence of vascular complications in extra-renal districts(0.5, 1 and 2 years follow up plus extended 4 yrs)

研究者

发起方
Azienda Unità Sanitaria Locale di Piacenza
申办方类型
Other

研究点 (1)

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