跳至主要内容
临床试验/NCT00279955
NCT00279955已完成不适用

Program to Access and Review Trending Information and Evaluate Correlation to Symptoms in Patients With Heart Failure

Medtronic Cardiac Rhythm and Heart Failure0 个研究点目标入组 1,024 人开始时间: 2004年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,024
主要终点
Occurrence of Heart Failure (HF) Related Adverse Event (AE)

研究概览

简要总结

The purpose of this study is to determine the value of diagnostic data obtained from Medtronic implantable cardioverter defibrillators (ICDs) with cardiac resynchronization therapy (CRT) to evaluate cardiovascular and heart failure related adverse events and health care utilization.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patients who meet the ICD indications
  • Patients with Class III or IV heart failure.
  • Patients receiving or who received a Medtronic CRT ICD within the previous 3 months.
  • Patient must sign and date informed consent, and be 18 years of age or greater.
  • Patient must be available for follow up visits, and be willing and able to comply with study protocol.

排除标准

  • Patient with acute myocardial infarction (MI), coronary artery bypass graft surgery (CABG) or percutaneous coronary angioplasty (PTCA)/stent within the last month.
  • Patient with a mechanical right heart valve.
  • Patient with chronic (permanent) atrial arrhythmias.
  • Patient with life expectancy of less than 12 months.
  • Patient with status post heart transplant
  • Patient undergoing kidney dialysis
  • Patients enrolled in a concurrent study that may confound the results of the study.

结局指标

主要结局

Occurrence of Heart Failure (HF) Related Adverse Event (AE)

时间窗: From 6 month to the 12 month visit

Number of participates with HF realted adverse event will be reported. Time to the first HF related Adverse event in the "Follow-up Period" from the 6-month visit to the 12-month visit is compared between two risk groups. The goal was to test if there is a significant difference in time to first HF-related adverse event between two groups. A heart failure related (HF-related) adverse event is defined as an adverse event that results in a subject's worsening HF or related to the heart's inability to meet the metabolic demands of the body.

次要结局

  • Occurrence of Heart Failure (HF) Related Healthcare Utilization (HU)(6 month to the 12 month visit)
  • Occurrence of Heart Failure (HF) Related Pulmonary Congestion Event (PCE)(6 month to the 12 month visit)

研究者

发起方
Medtronic Cardiac Rhythm and Heart Failure
申办方类型
Industry
责任方
Sponsor

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