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NCT05834803Recruiting

Effects of Percutaneous Transluminal Renal Angioplasty of Atherosclerotic Renal Artery Stenosis in High-Risk Patients.

Effects of Percutaneous Transluminal Renal Angioplasty of Atherosclerotic Renal Artery Stenosis in High-Risk Patients - a Danish Nationwide Randomized Sham-Controlled Study.

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

The goal of this clinical trial is to investigate whether percutaneous transluminal renal angioplasty (PTRA) with stent placement of atherosclerotic renal artery stenosis is beneficial in high-risk patients selected according to the criteria used in the DAN-PTRAI study. The main questions the trial aims to answer are whether renal artery stenting in addition to optimal medical therapy, compared with a sham procedure and optimal medical therapy, has beneficial effects on: * Blood pressure (primary outcome: 24-hour ambulatory systolic blood pressure at 6 months) * Kidney function * Hospitalizations for heart failure

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
3 Apr 2023
Start date
26 Jun 2023
Primary completion date
1 Jun 2027
Lead sponsor
University of Aarhus
NCT number
NCT05834803

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 26 Jun 2023 to the primary completion date, 1 Jun 2027
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Fibromuscular dysplasia or other non-atherosclerotic renal artery stenosis known to be present prior to randomization.
  • Previous kidney transplant.
  • Previous PTRA with stent placement.
  • Presence of a renal artery stenosis not amenable for treatment with a stent.
  • Intolerance to any antithrombotic treatment.
    • Patients who are not eligible for randomization but treated with renal artery stenting outside the protocol are followed according to the DAN-PTRAII protocol in order to account for all PTRA treatments performed in Denmark in the study period.
    • Patients treated with renal artery stenting without randomization in the study period include patients with:

Other illness

  • Treatment-resistant heart failure episodes presumed caused by renovascular disease.
  • Rapidly declining kidney function/acute kidney failure approaching the need for dialysis presumed caused by renovascular disease.
  • Treatment-resistant heart failure episodes presumed caused by renovascular disease.
  • Rapidly declining kidney function/acute kidney failure approaching the need for dialysis presumed caused by renovascular disease.
  • At least one of the listed high-risk clinical syndromes AND one or more significant atherosclerotic renal artery stenoses defined as a stenosis of 50-69% by catheter-based angiography with:
    • a mean translesional gradient of ≥10 mmHg, or
    • a systolic translesional gradient of ≥20 mmHg, or
    • a renal fractional flow reserve (Pd/Pa) of ≤0.80

Other

  • Unable to provide informed consent.
  • Pregnancy or unknown pregnancy status in female of childbearing potential.
  • Kidney size \<7 cm (pole to pole length) supplied by target vessel.

Who the study is looking for

  • One or more severe atherosclerotic renal artery stenoses defined as a stenosis ≥70% by catheter-based angiography.
  • In addition, at least one of the following high-risk clinical syndromes:
    • Resistant hypertension with average 24-hour ambulatory systolic blood pressure ≥150 mmHg despite ≥3 antihypertensive drugs including a diuretic, if tolerated, and each prescribed at optimal doses.
    • Rapidly declining kidney function with a reduction in estimated GFR of \>5 mL/min per 1.73m2 per year and average 24-hour ambulatory systolic blood pressure ≥140 mmHg despite ≥3 antihypertensive drugs including a diuretic, if tolerated, and each prescribed at optimal doses.
    • Hospital admissions with acute decompensated heart failure (≥2 hospitalizations for heart failure or ≥1 hospitalization for sudden, "flash" pulmonary edema) with no obvious explanations such as nonadherence, left ventricular ejection fraction \<40%, or valvular heart disease and average 24-hour ambulatory systolic blood pressure ≥140 mmHg despite ≥3 antihypertensive drugs including a diuretic, if tolerated, and each prescribed at optimal doses.
    • All 24-hour ambulatory blood pressure measurements are performed after nurse-administered medication.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Aarhus University Hospital
Coordinator of this site? Confirm its status
Aarhus NDenmarkRecruiting
Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting
Odense University Hospital
Coordinator of this site? Confirm its status
Odense CDenmarkRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.