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

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.

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2008/091/000204

Enrollment

2000

Registered

2009-02-11

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Interventions

Intervention1: Not applicable: Not applicable Control Intervention1: Not applicable: Not applicable

Eligibility

Inclusion criteria

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) 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

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

Design outcomes

Primary

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

Measure

Time frame

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

—

Secondary

Measure	Time frame
Not applicableTimepoint: Not applicable	—

Countries

India

Contacts

Public ContactRajesh Radhakrishnan

India Medtronic Pvt ltd

rajesh.radhakrishnan@medtronic.com912233074700

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026