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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Molecular Imaging of Myocardial Fibrosis in Cardiac AmyloidosisAmyloid Neuropathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, amyloidosis, disease, familial amyloid neuropathy, hereditary amyloidosis, hereditary disease, inborn errors of metabolism, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficienciesActive, not recruitingPhase 32026-07-06NCT05619302

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OrganizationsLinked trials
Brigham and Women's Hospital378

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Research sitesCityCountryLinked trials
Brigham and Women's HospitalBostonUnited States511