Plain-English translation of NCT03428048 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Coronary Artery Disease research guide →The NEXUS Registry is a long-term study that follows adults who receive treatment for coronary artery disease (blocked heart arteries) or atrial fibrillation (an irregular heartbeat). The study collects information about how patients feel and function after their procedures—including angiography, stent placement, or ablation therapy—over up to ten years. Researchers use this information to understand what works best and continuously improve the quality of care.
Many patients receive heart procedures, but doctors need better data on how well these treatments work and how they affect patients' daily lives over time. This registry bridges the gap between national heart care data and local hospital information, helping doctors identify what improves outcomes and quality of life for heart patients.
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You would complete health surveys at baseline (right before or after your heart procedure), then again at six months and once yearly for up to ten years. The surveys ask how you are feeling, your ability to do daily activities, and any symptoms you are experiencing. Most of the information comes from routine care and your medical records, so participation fits into your normal hospital visits and follow-up appointments.
AI-generated summary from trial data · Jul 4, 2026 · Not medical advice
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