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Revascularization of Renal Artery Stenosis Versus Medical Therapy for the Treatment of Ischemic Nephropathy (NITER)

Primary Purpose

Atherosclerosis, Chronic Kidney Disease, Hypertension, Renovascular

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Medical treatment
PTRS
renal artery stent
renal artery stent
Sponsored by
Azienda Unità Sanitaria Locale di Piacenza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atherosclerosis focused on measuring Angioplasty, Atherosclerotic reno vascular disease (ARVD), Cardio- and cerebro- vascular comorbidity, End stage renal disease (ERSD), kidney diseases, High blood pressure, Hypertension, Ischemic nephropathy, Percutaneous transluminal renal artery stenting (PTRS), Randomized controlled trials, Renal artery stenosis (RAS), Renal insufficiency, Vascular diseases

Eligibility Criteria

45 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Sites / Locations

  • Divisione di Nefrologia e Dialisi, "Guglielmo da Saliceto" Hospital, Azienda USL Piacenza

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

B:PTRS

A:medical therapy

Arm Description

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

hypotensive drugs, statins and antiplatelet therapy

Outcomes

Primary Outcome Measures

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)

Secondary Outcome Measures

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

Full Information

First Posted
December 1, 2009
Last Updated
December 1, 2009
Sponsor
Azienda Unità Sanitaria Locale di Piacenza
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1. Study Identification

Unique Protocol Identification Number
NCT01023373
Brief Title
Revascularization of Renal Artery Stenosis Versus Medical Therapy for the Treatment of Ischemic Nephropathy
Acronym
NITER
Official Title
Phase 4 Study of Medical Therapy Versus Medical Therapy Plus Renal Artery Stenting in Preventing the Progression of Renal Failure in Atherosclerotic Renovascular Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2009
Overall Recruitment Status
Unknown status
Study Start Date
October 2003 (undefined)
Primary Completion Date
September 2008 (Anticipated)
Study Completion Date
May 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Azienda Unità Sanitaria Locale di Piacenza

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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: 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 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis, Chronic Kidney Disease, Hypertension, Renovascular, Ischemic Nephropathy, Renal Artery Stenosis
Keywords
Angioplasty, Atherosclerotic reno vascular disease (ARVD), Cardio- and cerebro- vascular comorbidity, End stage renal disease (ERSD), kidney diseases, High blood pressure, Hypertension, Ischemic nephropathy, Percutaneous transluminal renal artery stenting (PTRS), Randomized controlled trials, Renal artery stenosis (RAS), Renal insufficiency, Vascular diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
B:PTRS
Arm Type
Experimental
Arm Description
B: the same medical therapy, as previously described in group A, associated with PTRS
Arm Title
A:medical therapy
Arm Type
Active Comparator
Arm Description
hypotensive drugs, statins and antiplatelet therapy
Intervention Type
Drug
Intervention Name(s)
Medical treatment
Intervention Description
hypotensive drugs, statins and anti-platelets
Intervention Type
Procedure
Intervention Name(s)
PTRS
Intervention Description
Percutaneous transluminal renal artery stenting. The same medical therapy, as in group A, plus PTRS
Intervention Type
Device
Intervention Name(s)
renal artery stent
Intervention Description
Non-drug intervention, percutaneous transluminal renal artery stent angioplasty
Intervention Type
Device
Intervention Name(s)
renal artery stent
Intervention Description
Adding the renal artery stenting (in group B) to the optimal medical therapy (as in group A) that includes hypotensive drugs, statins and antiplatelet therapy
Primary Outcome Measure Information:
Title
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)
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs
Secondary Outcome Measure Information:
Title
Systolic and diastolic blood pressure values at 0.5, 1 and 2 yrs follow up, with an extended follow up after 2 yrs
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs
Title
Number of hypotensive drugs
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs
Title
Results of renal scintigraphy
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs
Title
Incidence of complications due to interventional manoeuvres
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs
Title
Changes in the incidence of vascular complications in extra-renal districts
Time Frame
0.5, 1 and 2 years follow up plus extended 4 yrs

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberto Scarpioni
Organizational Affiliation
Divisione Nefrologia e Dialisi, "Guglielmo da Saliceto" Hospital, Azienda USL Piacenza, Italy
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emanuele Michieletti
Organizational Affiliation
U.O. Radiologia II "Guglielmo da Saliceto" Hospital, Piacenza
Official's Role
Principal Investigator
Facility Information:
Facility Name
Divisione di Nefrologia e Dialisi, "Guglielmo da Saliceto" Hospital, Azienda USL Piacenza
City
Piacenza
ZIP/Postal Code
29100
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
16245247
Citation
Scarpioni R, Michieletti E, Cristinelli L, Ugolotti U, Scolari F, Venturelli C, Cancarini G, Pecchini P, Malberti F, Maroldi R, Rozzi G, Olivetti L. Atherosclerotic renovascular disease: medical therapy versus medical therapy plus renal artery stenting in preventing renal failure progression: the rationale and study design of a prospective, multicenter and randomized trial (NITER). J Nephrol. 2005 Jul-Aug;18(4):423-8.
Results Reference
result

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Revascularization of Renal Artery Stenosis Versus Medical Therapy for the Treatment of Ischemic Nephropathy

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