Cardiomyopathy is a primary heart muscle disease characterized by a progressive dilation and dysfunction of either the left or both ventricles. This makes it harder for the heart to pump blood to the rest of the body. It can lead to heart failure, blood clots, valve problems, cardiac arrest and sudden death. There are several types of cardiomyopathy such as dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic right ventricular dysplasia and unclassified cardiomyopathy. It can be treated with the help of medications, surgically implanted devices, or a heart transplant. This book elucidates the concepts and innovative models around prospective developments with respect to the clinical management of cardiomyopathy. Different approaches, evaluations, methodologies, and advanced studies on the topic have been included herein. Scientists and students actively engaged in this field will find this book full of crucial and unexplored concepts.