PANARM HF : A clinical registry to understand the disease profiles of patients who suffer from cardiac arrhythmias and/or heart failure and to understand the diagnosis and treatment pathway of these patients

Phase 4

Completed

Conditions: Health Condition 1: null- Patient with heart failure &/or symptomatic cardiac arrhythmias or asymptomatic left ventricular dysfunction patients

Registration Number: CTRI/2008/091/000204

Lead Sponsor: India Medtronic Pvt Ltd

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 2000

Inclusion Criteria

Patients with one or more of the following symptoms secondary to cardiac arrhythmias &/or heart failure :

Syncope

Pre-syncope

Palpitations

Dyspnea

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

Exclusion Criteria

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

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To understand the patient enrollment patterns, patient referral patterns and patient interventional therapy prescription patterns for the study population and sub-groups <br/ ><br>To understand the demographic & symptom profile of the study population and sub-groups <br/ ><br>To understand the cardiac arrhythmia and heart failure patterns and cardiovascular system parameter profile of the study population and sub-groups <br/ ><br>To understand the disease etiology profile of the study population and sub-groupsTimepoint: At enrollment

Secondary Outcome Measures