IU School of Medicine | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Hospital @ Home Model of Care for Cirrhosis	Decompensated Cirrhosis	Recruiting	Not applicable	2026-09-22		NCT06396897
Pediatric Cardiomyopathy Mutation Analysis	Cardiomegaly, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypertrophy, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, dilated cardiomyopathy, heart disorder, heart failure, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, left ventricular noncompaction, restrictive cardiomyopathy, subvalvular aortic stenosis	Recruiting	Not stated	2026-06-22		NCT02432092
Pathogenetic Basis of Aortopathy and Aortic Valve Disease	Abnormalities, Multiple, Acute Aortic Syndrome, Aneurysm, Aneurysm, Ascending Aorta, Aortic Aneurysm, Giant Congenital, Aortic Dissection, Bicuspid Aortic Valve Disease, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dissection, Blood Vessel, Dissection, Thoracic Aorta, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Loeys-Dietz syndrome, Male Urogenital Diseases, Marfan syndrome, Musculoskeletal Abnormalities, PHACE syndrome, Sex Chromosome Disorders, Shprintzen Golberg craniosynostosis, Skin Abnormalities, Skin and Connective Tissue Diseases, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, aortic aneurysm, aortic aneurysm, familial thoracic 1, aortic disorder, aortic valve disorder, arterial tortuosity syndrome, bone disorder, cardiovascular disorder, chromosomal disorder, congenital contractural arachnodactyly, congenital heart disease, connective tissue disorder, cutis laxa, autosomal recessive, type 1A, disorder of sexual differentiation, endocrine system disorder, familial thoracic aortic aneurysm and aortic dissection, gonadal disorder, gonadal dysgenesis, heart disorder, heart valve disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, sex chromosome disorder of sex development, skin disorder, thoracic aortic aneurysm, vascular disorder, vascular hemostatic disease	Active, not recruiting	Not stated	2026-02-13		NCT03440697