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临床试验/NCT02282683
NCT02282683Unknown2 期

Long-term Prednisone Use in Patients With Advanced Heart Failure (ACCF/AHA Stage D) and Hyperuricemia

Hebei Medical University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2013年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
90
试验地点
1
主要终点
Mortality within 12 months

研究概览

简要总结

Patients with advanced (ACCF/AHA stage D) heart failure and hyperuricemia have high one-year mortality. Currently, there was no evidence-based therapy such as mechanically assisted circulatory support available in China. The investigators found glucocorticoid treatment such as prednisone could improve cardiac performance, potentiate renal responsiveness to diuretics in such patients. Therefore, it could be used as bridge therapy to help ACE inhibitors or beta blocker titration. With its help, most of the patients with stage D heart failure could be titrated to higher dose of ACE inhibitors and beta blockers during hospitalization. However, the efficacy of long-term, low-dose of prednisone use in such patients with limited life expectancy remain unclear. Therefore, the investigators designed this study to observe whether putting low-dose of prednisone on the patients with stage D heart failure for long term could further improve their survival. All patients will receive prednisone treatment during hospitalization and receive maximum tolerated guideline-directed medical therapy (GDMT). After discharge from hospital, the patients will be randomized to receive long-term, low-dose prednisone treatment or standard GDMT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Repeated (>2) hospitalizations or ED visits for HF in the past year
  • Inability to exercise including exertion limited, exertion intolerance, resting symptoms or inotrope dependent
  • Left ventricular ejection fraction ≤35%
  • Serum uric acid level ≥500μmol/L
  • Received prednisone treatment during hospitalization period and And more 5 of the followings
  • Progressive deterioration in renal function (e.g., rise in BUN and creatinine)
  • Weight loss without other cause (e.g., cardiac cachexia)
  • Intolerance to ACE inhibitors due to hypotension and/or worsening renal function
  • Intolerance to beta blockers due to worsening HF or hypotension
  • Frequent systolic blood pressure <90 mm Hg
  • Recent need to escalate diuretics to maintain volume status, often reaching daily furosemide equivalent dose >160 mg/d and/or use of supplemental thizide therapy
  • Progressive decline in serum sodium, usually to <133 mEq/L
  • Gastrointestinal symptoms (abdominal discomfort, nausea, poor appetite), disabling ascites, or severe lower-extremity edema

排除标准

  • Any condition (other than heart failure) that could limit the use of prednisone
  • Any concurrent disease that likely limits life expectancy;
  • Active myocarditis, or an hypertrophic obstructive or restrictive cardiomyopathy;
  • Myocardial infarction, stroke, unstable angina, or cardiac surgery within the previous 3 months;
  • Indication for hemodialysis
  • Uncontrolled systolic blood pressure > 160 mmHg
  • Complex congenital heart disease
  • Poorly controlled diabetes

研究组 & 干预措施

Prednisone

Experimental

Prednisone (10 to 20 mg/day, orally) combined with maximum tolerated guideline-directed medical therapy for at least 12 months.

干预措施: prednisone (Drug)

结局指标

主要结局

Mortality within 12 months

时间窗: 12 months

次要结局

  • Change from baseline in serum uric acid(month 6 and month 12)
  • Change from baseline in serum creatinine(month 6 and month 12)
  • Event-free survival time (defined as time to first hospitalization due to heart failure deterioration or death) within 12 months(12)
  • Survival time (defined as time to death) within 12 months(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kun-shen Liu M.D.

Professor

Hebei Medical University

研究点 (1)

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