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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
COhort for Bardet-Bield Syndrome and Alström Syndrome for Translational Research Monocentric Interventional StudyAbnormalities, Multiple, Alstrom syndrome, Bardet-Biedl syndrome, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, brain disorder, central nervous system disorder, central nervous system malformation, eye disorder, hereditary disease, hereditary motor and sensory neuropathy, hypothalamic disorder, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, retinitis pigmentosaRecruitingNot applicable2021-09-10NCT04461444