CTRI/2008/091/000204已完成4 期
PANARM HF -A prospective, multi-center, non-interventional to collect (at the referring physician stage), data pertaining to the demographic, cardiovascular and disease etiology profiles of patients who have symptomatic cardiac arrhythmias &/or left ventricular dysfunction with or without symptoms of heart failure.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 2,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Patients with one or more of the following symptoms secondary to cardiac arrhythmias &/or heart failure :
- •Pre-syncope
- •Palpitations
- •Fatigue and/or
- •Patients with Left Ventricular (LV) dysfunction ( Left Ventricular Ejection Fraction (LVEF) < 40%, as measured through echo) with or without one or more of the above mentioned symptoms
- •Patients for whom a completed Referring Physician Case Report Form (RP CRF) with test results are available
- •Patients who have signed and dated a Patient Data Release Form specified in this study plan
- •Patients who are at least 18 years of age at the time of enrollment
排除标准
- •Patients with heart failure arising out of primary valvular disease with stenotic lesions
- •Patients with acute myocardial infarction (< 40 days), patients with electrolyte imbalance, acute pulmonary embolism, pneumothorax and other acute syndromes/events that are reversible
- •Patients with recent percutaneous coronary intervention or cardiovascular surgery (< 40 days in the past)
- •Patients whose symptoms are not due to a cardiovascular cause
- •Patients in whom the only symptoms are palpitation due to premature atrial contractions (PAC) and/or premature ventricular contractions (PVC) and who do not meet any of the other inclusion criteria
- •Patients with Coronary Artery Disease (CAD) but with no history of heart failure (Stage B or greater) and/or LV dysfunction and/or arrhythmia
- •Unwillingness or inability to cooperate or give voluntary consent to participate in the Study
研究者
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