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Clinical Trials/NCT03686358
NCT03686358
Completed
Not Applicable

Evaluation of Renal Angioplasty on Atherosclerotic Stenosis Since 2010

Rennes University Hospital1 site in 1 country80 target enrollmentMay 29, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Renal Angioplasty on Atherosclerotic Stenosis
Sponsor
Rennes University Hospital
Enrollment
80
Locations
1
Primary Endpoint
Composite endpoint at 3 years
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The interest of renal angioplasty in the nosological framework of atherosclerotic stenosis has been significantly challenged by STAR and ASTRAL clinical trials in 2009, confirmed by the CORAL study in 2014.

These studies did not show any benefit of the gesture on renal function, morbidity and cardiovascular mortality or the tension control. The aim of the study is to evaluate renal angioplasty on atherosclerotic stenosis.

Detailed Description

Previous studies did not concern the indication of renal angioplasty in some high-risk situations, such as malignant or resistant renal vascular hypertension, OAP (Acute pulmonary oedema) flash or acute renal failure of ischemic origin. There is no work in the literature that has studied retrospectively the evolution of angioplasty practices renal artery disease on atherosclerotic stenosis since 2009, nor their remote results of the gesture.

Registry
clinicaltrials.gov
Start Date
May 29, 2017
End Date
July 12, 2017
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Rennes University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • OAP flash: hospitalization for Acute congestive heart failure without any other identified etiology than renal artery stenosis
  • Resistant arterial hypertension under treatment including a diuretic
  • Acute renal failure or ischemic renal failure quickly progressive
  • Radiological criteria: renal ischemia visualized at arterial time of angio-CT or renal angio-MRI

Exclusion Criteria

  • Renal transplant patients
  • Patients with another etiology of secondary hypertension, including fibro-muscular dysplasia of renal artery
  • Restenosis on stent, angioplasty of accessory renal artery
  • Patients subject to legal protection (safeguard of justice, guardianship) and persons deprived of liberty
  • Patients objecting to participate to the study

Outcomes

Primary Outcomes

Composite endpoint at 3 years

Time Frame: The inclusion day

Composite endpoint at 3 years : * Cardiovascular or renal mortality, * Initiation of a renal replacement therapy or estimated glomerular filtration rate decrease of more than 50%, Cardiovascular morbidity: hospitalization for congestive heart failure, myocardial infarction, myocardium, stroke.

Study Sites (1)

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