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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome22q11.2 deletion syndrome, Abnormalities, Multiple, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, DiGeorge syndrome, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, Musculoskeletal Abnormalities, cardiovascular disorder, chromosomal disorder, congenital heart disease, endocrine system disorder, heart disorder, hereditary disease, hypoparathyroidism, lymphatic system disorder, musculoskeletal system disorder, parathyroid gland disorderRecruitingNot stated2026-07-29NCT00556530
Non-Invasive Brain Stimulation to Improve Language in Down Syndrome.Abnormalities, Multiple, Charcot-Marie-Tooth disease type 1F, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Down syndrome, Neurobehavioral Manifestations, Neurologic Manifestations, chromosomal disorder, hereditary disease, intellectual disability, nervous system disorderRecruitingNot applicable2026-07-24NCT07044804