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Results for “Epileptic Encephalopathy, Neonatal-onset”

8 trials

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Showing 8 of 8 results

Not applicableUnknownNCT03934268
What this trial is testing

A Cohort Study on the Prognosis of Neonatal KCNQ2 Gene-associated Epileptic Encephalopathy

Who this might be right for
SeizuresSeizure DisorderSeizure Newborn+5 more
Children's Hospital of Fudan University 100
Not applicableStudy completedNCT05687474
What this trial is testing

Baby Detect : Genomic Newborn Screening

Who this might be right for
Congenital Adrenal HyperplasiaFamilial Hyperinsulinemic Hypoglycemia 1Phosphoglucomutase 1 Deficiency+121 more
Centre Hospitalier Universitaire de Liege 6,824
Not applicableEnrolling By InvitationNCT03655223
What this trial is testing

Early Check: Expanded Screening in Newborns

Who this might be right for
Spinal Muscular AtrophyFragile X SyndromeFragile X - Premutation+182 more
RTI International 30,000
Early research (Phase 1)Looking for participantsNCT06700811
What this trial is testing

Ketogenic Diet for Prevention of Epileptic Spasms in Infantile Onset Genetic Epilepsies

Who this might be right for
Developmental and Epileptic EncephalopathiesEpileptic SpasmsGenetic Epilepsy+1 more
Heather Olson 10
Not applicableStudy completedNCT00006176
What this trial is testing

Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies

Who this might be right for
Familial Dementia With Neuroserpin Inclusion BodiesNervous System Heredodegenerative Disorder
National Human Genome Research Institute (NHGRI) 100
Not applicableLooking for participantsNCT04802135
What this trial is testing

Creation of a Register of Patients With Neonatal-onset Epileptic Encephalopathy

Who this might be right for
Epileptic Encephalopathy
Assistance Publique Hopitaux De Marseille 200
Not applicableLooking for participantsNCT06500260
What this trial is testing

CNKSR2 Natural History Study

Who this might be right for
Developmental DysphasiaEpileptic Encephalopathy, Childhood-OnsetX-Linked Intellectual Disability
University of California, San Francisco 15
Not applicableLooking for participantsNCT01793168
What this trial is testing

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Who this might be right for
Rare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more
Sanford Health 20,000