Clinical Trials on Weber Syndrome

Total 19 results

    • NCT04447846
      Recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT02332655
      Active, not recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT04517565
      Recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT04717427
      Recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT01425944
      Active, not recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT03047980
      Active, not recruiting
      Conditions: Sturge-Weber Syndrome
    • NCT01997255
      Withdrawn
      Conditions: Sturge Weber Syndrome
    • NCT02080624
      Completed
      Conditions: Sturge- Weber Syndrome
    • NCT00610402
      Completed
      Conditions: Sturge - Weber Syndrome (SWS)
    • NCT01533376
      Terminated
      Conditions: Sturge Weber Syndrome; Port-wine Mark
    • NCT01345305
      Completed
      Conditions: Sturge-Weber Syndrome
    • NCT00639730
      Completed
      Conditions: Epilepsy; Sturge Weber Syndrome
    • NCT04735601
      Recruiting
      Conditions: Glaucoma
    • NCT01364857
      Unknown status
      Conditions: Port Wine Stain; Klippel Trenaunay Syndrome; Parkes Weber Syndrome
    • NCT04344626
      Recruiting
      Conditions: Epilepsy; Focal Cortical Dysplasia; Tuberous Sclerosis; Hemimegalencephaly; Polymicrogyria; Rasmussen Encephalitis; Sturge-Weber Syndrome; Gliosis; Stroke; Tumor, Brain
    • NCT03001180
      Recruiting
      Conditions: Vascular Anomaly; Generalized Lymphatic Anomaly; Kaposiform Hemangioendothelioma; Kaposiform Lymphangiomatosis; Gorham-Stout Disease; Klippel Trenaunay Syndrome; Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
    • NCT02399527
      Recruiting
      Conditions: Lymphatic Malformation; Generalized Lymphatic Anomaly (GLA); Central Conducting Lymphatic Anomaly; CLOVES Syndrome; Gorham-Stout Disease ("Disappearing Bone Disease"); Blue Rubber Bleb Nevus Syndrome; Kaposiform Lymphangiomatosis; Kaposiform Hemangioendothelioma/Tufted Angioma; Klippel-Trenaunay Syndrome; Lymphangiomatosis
    • NCT01761981
      Unknown status
      Conditions: Haemorrhagic Hereditary Telangiectasia
    • NCT01031992
      Completed
      Conditions: Hereditary Hemorrhagic Telangiectasia