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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical Registry Investigating Bardet-Biedl SyndromeAbnormalities, Multiple, Bardet-Biedl syndrome, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, brain disorder, central nervous system disorder, eye disorder, hereditary disease, hypothalamic disorder, nervous system disorder, retinitis pigmentosaRecruitingNot stated2022-07-19NCT02329210