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Registry Following Balloon Widening of Kidney Arteries in High Blood Pressure

Records outcomes of balloon kidney artery widening in high-risk people with renovascular hypertension.

Plain-language title generated from the registry record
Registry title: A Prospective Danish National Registry of PTRA in Patients With Renovascular Hypertension

Key facts

Where
Aalborg, Aarhus N, Glostrup Municipality, Holbæk, and Odense C, DenmarkSee the 5 sites

Where in Denmark

  • Aalborg University HospitalAalborg, DenmarkTaking people
  • Aarhus University HospitalAarhus N, DenmarkTaking people
  • Glostrup University Hospital/ RigshospitaletGlostrup Municipality, DenmarkTaking people
  • Holbaek HospitalHolbæk, DenmarkTaking people
  • Odense University HospitalOdense C, DenmarkTaking people

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Trial details

Who runs it
University of Aarhus
Trial code
NCT02770066
Record updated
18 December 2025
Original description
A prospective Danish national registry of percutaneous transluminal renal angioplasty (PTRA) in high-risk patients with renal artery stenosis selected on the basis of common national criteria, and with a common follow-up protocol for all three Danish centres offering PTRARead full original descriptionShow less

A Prospective Danish National Registry of Percutaneous Transluminal Renal Angioplasty in Patients With Renovascular Hypertension

A prospective Danish national registry of percutaneous transluminal renal angioplasty (PTRA) in high-risk patients with renal artery stenosis selected on the basis of common national criteria, and with a common follow-up protocol for all three Danish centres offering PTRA

Inclusion: All of the following:; At least one of the above eligibility criteria; Duplex doppler ultrasonography or renography investigations consistent with hemodynamically significant renal artery stenosis; CT angiography or renal arteriography with angiographic renal artery stenosis of ≥ 70 % reduction of the luminal diameter in at least one projection.

Exclusion: If angiography/arteriography, ultrasonography or renography is consistent with bilateral significant renal artery stenosis and only one side is treated with PTRA; PTRA of a renal artery supplying a kidney which pre-PTRA handles ≤ 10% of the total kidney function (with no blockage of the renin-angiotensin system) and has a kidney size < 7 cm (length).

Eligibility criteria; True resistant hypertension (≥ 3 antihypertensive drugs including a diuretic, if tolerated, and each prescribed at optimal doses) and uncontrolled blood pressure confirmed by 24-hour ambulatory blood pressure monitoring. The 24-hour ambulatory blood pressure monitoring is performed after nurse-administered medication and blood pressure measurements are performed hourly. If the average 24-hour ambulatory systolic blood pressure is ≥ 130 mmHg the patient can be evaluated for renal artery stenosis; Hypertension and intolerance or side effects of the antihypertensive treatment. Hypertension is confirmed by 24-hour ambulatory blood pressure monitoring. The 24-hour ambulatory blood pressure monitoring is performed after nurse-administered medication and blood pressure measurements are performed hourly. If the average 24-hour ambulatory systolic blood pressure is ≥ 130 mmHg the patient can be evaluated for renal artery stenosis; Progressive renal insufficiency (a reduction in eGFR > 5 ml/min/1,73 m2 per year) in patients with bilateral renal artery stenosis or in patients with renal artery stenosis and only one kidney; Recurrent heart failure/pulmonary edema and resistant hypertension (≥ 3 antihypertensive drugs including a diuretic, if tolerated, and each prescribed at optimal doses) that may not be attributed to non-compliance, reduced left heart ventricular ejection fraction/heart valve disease or other obvious explanations (atrial fibrillation, fever, hyperthyroidism etc.). If the average 24-hour ambulatory systolic blood pressure is ≥ 130 mmHg after nurse-administered medication the patient can be evaluated for renal artery stenosis; Younger patients (< 40 years) with hypertension (24-hour ambulatory blood pressure monitoring ≥ 130/80 mmHg after nurse-administered medication ).

ClinicalTrials.gov NCT02770066