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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Analysis of the Evolution of SUVmax by Quantitative Analysis Method of Bisphosphonate ScintigraphyAmyloid Neuropathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, amyloidosis, 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 deficienciesRecruitingNot applicable2026-08-20NCT04849754

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Research sitesCityCountryLinked trials
Hôpital Privé Le BoisLilleFrance6