Clinical Trials on Malformations of Cortical Development

Total 89 results





    • NCT02451696
      Completed
      Conditions: Epilepsy; Tuberous Sclerosis Complex; Focal Cortical Dysplasia
    • NCT00687024
      Completed
      Conditions: Focal Cortical Dysplasia; Epilepsy
    • NCT03198949
      Recruiting
      Conditions: Epilepsy and Focal Cortical Dysplasia II
    • NCT02261753
      Terminated
      Conditions: Cortical Dysplasia
    • NCT02890641
      Recruiting
      Conditions: Cortical Dysplasia-Focal Epilepsy Syndrome
    • NCT00041600
      Unknown status
      Conditions: Epilepsy; Seizures; Cognition Disorders; Neuronal Migration Disorders
    • NCT04344626
      Recruiting
      Conditions: Epilepsy; Focal Cortical Dysplasia; Tuberous Sclerosis; Hemimegalencephaly; Polymicrogyria; Rasmussen Encephalitis; Sturge-Weber Syndrome; Gliosis; Stroke; Tumor, Brain
    • NCT02654340
      Recruiting
      Conditions: Hypomelanotic Macules; Facial Angiofibroma; Shagreen Patches; Ungual Fibromas; Cortical Dysplasia; Cardiac Rhabdomyoma; Lymphangioleiomyomatosis; Renal Angiomyolipoma; Subependymal Giant Cell Astrocytoma
    • NCT00552045
      Completed
      Conditions: Epilepsy; Localization-related Epilepsy; Infantile Spasms; Lennox-Gastaut Syndrome; Polymicrogyria; Periventricular Heterotopias
    • NCT03321240
      Recruiting
      Conditions: Refractory Epilepsy; Focal Epilepsy; Focal Cortical Dysplasia
    • NCT00686530
      Withdrawn
      Conditions: Brain Malformation
    • NCT03255369
      Unknown status
      Conditions: ZIKA VIRUS INFECTION; Child Development; Microcephaly
    • NCT03548779
      Recruiting
      Conditions: Epilepsy; Seizure; Neuromuscular Diseases; Brain Malformation; Intellectual Disability; Autism Spectrum Disorder; Hypotonia; Inborn Errors of Metabolism; Movement Disorders; Genetic Disease; Development Delay; Chromosome Abnormality; Hearing Loss; Dysmorphic Features; Skeletal Dysplasia; Congenital Abnormality; Microcephaly; Macrocephaly
    • NCT04463316
      Recruiting
      Conditions: Prader-Willi Syndrome; PWS-like Syndrome; Silver Russel Syndrome; Congenital Hypopituitarism; Klinefelter (XXY-)Syndrome; Congenital Adrenal Hyperplasia; XXXXY Syndrome; XXYY Syndrome; XXXX Syndrome (Tetra-X Syndrome); Disorders of Sex Development; Turner Syndrome; 46, XY DSD; Tuberous Sclerosis; Neurofibromatosis; Albright Hereditaire Osteodystrofie; Cornelia de Lange Syndrome; Saethre-Chotzen Syndrome; 17p- Deletiesyndrome; VCF Syndrome; POLR3A Mutatie; Ohdo Syndrome; Jacobsen Syndrome / 11 q Syndrome; Myrhe Syndrome; CHARGE Syndrome; 1q25-32 Deletie; Bardet Biedl Syndrome; Rett Syndrome; 22q11 Deletion Syndrome; Allan-Herndon-Dudley Syndrome; Kallmann Syndrome; Rare Bone Disorders; Noonan Syndrome; Williams-Beuren Syndrome
    • NCT00001639
      Completed
      Conditions: Abnormalities; Failure to Thrive; Mental Retardation; Microcephaly
    • NCT03922594
      Recruiting
      Conditions: Microcephaly; Congenital Infection
    • NCT01151462
      Withdrawn
      Conditions: Hearing Loss; Mental Retardation; Microcephaly; Chorioretinitis
    • NCT03651687
      Recruiting
      Conditions: Microcephaly
    • NCT02943304
      Recruiting
      Conditions: Microcephaly; Mental Retardation
    • NCT04569149
      Recruiting
      Conditions: MOPDII; MOPDI; MOPDIII; Taybi Linder Syndrome; Meier-Gorlin Syndrome; Saul-Wilson Syndrome; Ligase 4 Syndrome; Lowry Wood Syndrome; Microcephalic Primordial Dwarfism
    • NCT04595513
      Recruiting
      Conditions: Tuberous Sclerosis Complex; Epilepsy
    • NCT04485104
      Not yet recruiting
      Conditions: Seizure in Participants With Tuberous Sclerosis Complex
    • NCT04285346
      Recruiting
      Conditions: Tuberous Sclerosis
    • NCT02741882
      Completed
      Conditions: Microcephaly
    • NCT04112537
      Active, not recruiting
      Conditions: Tuberous Sclerosis Complex