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临床试验/ACTRN12620000764932
ACTRN12620000764932尚未招募未知

Effect of Aggressive vs. Lenient Blood Pressure Control in Patients with Ventricular Tachycardia (VT) on Future VT and Death

Sachin Nayyar0 个研究点目标入组 120 人开始时间: 2020年7月27日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • 1. Age 18-year to 80-years.
  • 2. Heart failure due to ischemic or non-ischemic etiology of more than 3 months duration.
  • 3. Left ventricular ejection fraction <40%.
  • 4. History of spontaneous sustained VT.
  • 5. Have an implantable cardioverter defibrillator (ICD) or consent to have one.
  • 6. NYHA Class 1 -3.

排除标准

  • 1.VT related hospitalization within the last 3 weeks.
  • 2.VT ablation in last 3 months.
  • 3.Heart failure NYHA Class 4 or heart failure hospitalization within the last 3 weeks.
  • 4.Resting systolic BP < 90mmHg at lowest doses of heart failure medication.
  • 5.History of symptomatic systolic BP drop on standing.
  • 6.Exercise induced systolic BP > 180mmHg or <90mmHg.
  • 7.Known secondary cause of hypertension.
  • 8.eGFR less than 30ml/min.
  • 9.Intolerance to beta-blocker (equivalent to Metoprolol 12.5mg BD) (due to worsening of hypotension or heart failure).
  • 10.Left ventricular ejection fraction <10%.
  • 11.Suspected tachy-cardiomyopathy (arrhythmia as cause of heart failure).
  • 12.Acute coronary event or stroke within the last 3 months.
  • 13.Coronary revascularization within the last 3 months.
  • 14.Expected survival less than 3 years due to terminal non-cardiac illness.
  • 15.Severe pulmonary artery hypertension.
  • 16.Large pericardial effusion.
  • 17.Severe peripheral vascular disease or aortic aneurysm.
  • 18.Non-compliance to medication.
  • 19.Active alcohol or substance abuse.
  • 20.Pregnancy.
  • 21.Morbid obesity (BMI >40).
  • 22.Remote residence out of reach to clinic sites.
  • 23.Dementia or other cognitive impairment in ability to follow the protocol.
  • 24.Current participation in another trial.

研究者

发起方
Sachin Nayyar

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