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
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