跳至主要内容
临床试验/ISRCTN40476871
ISRCTN40476871已完成未知

Does allopurinol regress left ventricular hypertrophy in patients with treated essential hypertension?

The University of Dundee and NHS Tayside (UK)0 个研究点目标入组 72 人开始时间: 2014年10月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
72

研究概览

简要总结

2019 results in https://www.ncbi.nlm.nih.gov/pubmed/31268872 (added 22/07/2019)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged over 18 years
  • 2. Previously diagnosed with essential hypertension
  • 3. Been on stable antihypertensive therapy for at least 3 months prior to study screening
  • 4. Have screening ABPM (or home based BP monitoring if ABPM not tolerated) with daytime average systolic <135mmHg or 24-hour average systolic = 130mmHg
  • 5. Have screening echocardiography based diagnosis of LVH based on ASE criteria (males >115g/m2, females >95g/m2)

排除标准

  • 1. Documented intolerance to allopurinol
  • 2. Left ventricular ejection fraction <45% on echocardiography screening
  • 3. Severe aortic stenosis on echocardiography screening
  • 4. Already had gout or currently on allopurinol
  • 5. Severe hepatic disease
  • 6. Renal disease; CKD class 3B or worse
  • 7. On azathioprine, 6 mercaptopurine, or theophylline
  • 8. Malignancy (receiving active treatment) or other life threatening diseases
  • 9. Pregnant or lactating women
  • 10. Any contraindication to MRI (claustrophobia, metal implants, penetrative eye injury or exposure to metal fragments in eye requiring medical attention)
  • 11. Patients who have participated in any other clinical trial of an investigational medicinal product within the previous 30 days will be excluded
  • 12. Patients who are unable to give informed consent
  • 13. Any other considered by a study physician to be inappropriate for inclusion

研究者

发起方
The University of Dundee and NHS Tayside (UK)

相似试验