跳至主要内容
临床试验/EUCTR2012-001066-14-ES
EUCTR2012-001066-14-ES进行中(未招募)不适用

Sympathetic renal denervation versus increment of pharmacological treatment in resistant arterial hypertension

Consorci Mar Parc de salut de Barcelona ( Parc de Salut Mar)0 个研究点开始时间: 2012年6月12日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Subjects aged = 18 years and = 80 years.
  • 2.Subjects with diagnosed resistant arterial hypertension (office blood pressure = 140 and/or 90 mm Hg despite treatment with at least 3 antihypertensive drugs given at the maximum tolerated therapeutic dosage, being one of them a diuretic), with this therapeutic regimen maintained for at least the last 3 months.
  • 3.Office systolic blood pressure =150 mm Hg, with confirmation of resistance to treatment by 24h ambulatory blood pressure monitoring, with 24h-systolic blood pressure =140 mmHg being required to be included.
  • 4.Patients who have freely given informed consent in writing, after the nature of the study and the disclosure of their data have been explained to them.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 20
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 30

排除标准

  • 1.Secondary hypertension, renovascular disease included with appropriate tests according to investigator criteria (with the exceptions of chronic renal disease and obstructive sleep-apnea syndrome).
  • 2.Inability to perform magnetic resonance angiography or renal CT angiography (contrast allergy).
  • 3.Patients unlikely compliant with treatment (assessed according to Haynes-Sackett test).
  • 4.Patients currently on treatment with an aldosterone receptor blocker (spironolactone, eplerenone) or who had previously received one of such class of drugs and had been withdrawn due to lack of efficacy and/or adverse effects.
  • 5.Stage 3B, 4 or 5 of chronic renal disease (estimated glomerular filtration rate by MDRD equation < 45 mL/min/1.73m2).
  • 6.Pre-randomization serum potassium (K+) level = 5.5 mmol/L.
  • 7.Significant renal vascular anomalies.
  • 8.Pregnant women.
  • 9.Significant valvular heart disease.
  • 10.Major vascular event (myocardial infarction, unstable angina or cerebrovascular disease) < 6 months prior to study enrolment.

研究者

发起方
Consorci Mar Parc de salut de Barcelona ( Parc de Salut Mar)

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