Find NINDS Clinical Trials

Find NINDS Clinical Trials

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Returning 57 results
Study Title Location Statussort descending Disorders
Treatment Development of Triheptanoin (G1D) Texas Not Yet Recruiting Epilepsy, GLUT1DS1, Glut1 Deficiency Syndrome 1, Autosomal Recessive, Glucose Metabolism Disorders, Glucose Transport Defect, Glucose Transporter Type 1 Deficiency Syndrome, Glucose Transporter Protein Type 1 Deficiency Syndrome
Diet Treatment Glucose Transporter Type 1 Deficiency (G1D) Texas Not Yet Recruiting GLUT1DS1, Epilepsy, Glut1 Deficiency Syndrome 1, Autosomal Recessive, Glucose Metabolism Disorders, Glucose Transport Defect, Glucose Transporter Type 1 Deficiency Syndrome, Glucose Transporter Protein Type 1 Deficiency Syndrome
Distinct Mechanisms of Cognitive Behavioral Therapy Effects in Youth With Migraine Ohio Not Yet Recruiting Headache, Migraine, Migraine, Migraine Disorders, Headache
5-Cog Battery for Detecting Cognitive Impairment and Dementia New York Not Yet Recruiting Dementia, Cognitive Impairment, Mild Cognitive Impairment, Neurocognitive Disorders
Transcranial Magnetic Stimulation for BECTS California Not Yet Recruiting Benign Epilepsy With Centrotemporal Spikes, Language Problems, Learning Disorders
Natural History Study of Patients With Neurofibromatosis Type 2 Maryland* Recruiting Neurofibromatosis, Intracranial Central Nervous System Disorder, Neurologic Disorders, Brain Neoplasms
Neurobiology of Functional Movement Disorder and Non-Epileptic Seizures Multiple U.S. Locations* Recruiting Movement Disorders, Non-epileptic Seizures
Human Epilepsy Genetics--Neuronal Migration Disorders Study Multiple U.S. Locations Recruiting Epilepsy, Seizures, Cognition Disorders, Neuronal Migration Disorders
Biobanking of Rett Syndrome and Related Disorders Multiple U.S. Locations Recruiting Rett Syndrome, MECP2 Duplication, CDKL5, FOXG1 Disorders
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) Multiple U.S. Locations Recruiting Mitochondrial Disorders, Mitochondrial Genetic Disorders, Mitochondrial Diseases, Disorder of Mitochondrial Respiratory Chain Complexes, Deletion and Duplication of Mitochondrial DNA

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