NCT00865644
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cutaneous Neurofibromas, Genetic Diseases, Inborn, +15 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
Clinical trial condition
Neurofibromatoses
Explore clinical trials studying Neurofibromatoses. Study availability and eligibility vary by location and protocol.
143 public trials
20 recruiting studies
Neurofibromatoses trial results
Completed
Trial to Evaluate the Safety of Lovastatin in Individuals With Neurofibromatosis Type I (NF1)
NCT00352599
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +13 more
- Locations
-
- Semel Institute for Neuroscience and Human Behavior Los Angeles, California, United States
NCT00657202
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cutaneous Neurofibromas, Genetic Diseases, Inborn, +17 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT01851135
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +14 more
- Locations
-
- Assistance Publique - Hôpitaux de Paris (Hôpital Henri Mondor) Créteil, France
- Centre Hospitalier Universitaire de Nantes Nantes, France
Completed
Lapatinib Study for Children and Adults With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors
NCT00973739
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Cranial Nerve Neoplasms, +28 more
- Locations
-
- New York University School of Medicine New York, United States
NCT02479360
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +14 more
- Locations
-
- Neurofibromatosis Unit, Guys Hospital. London, United Kingdom
NCT02422732
- Conditions
- Communication Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslexia, +25 more
- Locations
-
- CHU Toulouse Toulouse, France
Completed
Pirfenidone in Treating Young Patients With Neurofibromatosis Type 1 and Plexiform Neurofibromas
NCT00053937
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +19 more
- Locations
-
- University of Alabama at Birmingham Comprehensive Cancer Center Birmingham, Alabama, United States
- Children's National Medical Center Washington D.C., District of Columbia, United States
- Children's Memorial Hospital - Chicago Chicago, Illinois, United States
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore, Maryland, United States
Completed
Reading Disability in Children With NF1
NCT02397967
- Conditions
- Communication Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslexia, +25 more
- Locations
-
- Hopital femme-mére-enfant, Hospices civils de lyon Lyon, France
- Hôpital Gui de Chauliac Montpellier, France
- CHU Hôtel-Dieu, Clinic of Dermatology Nantes, France
- AP-HP Hopital Armand Trousseau Paris, France
NCT00030043
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Cranial Nerve Neoplasms, +24 more
- Locations
-
- House Ear Institute Los Angeles, California, United States
- Huntington Medical Research Institutes Pasadena, California, United States
- Cochlear Corporation Englewood, Colorado, United States
Related conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (143)
- Heredodegenerative Disorders, Nervous System (143)
- Neoplasms by Histologic Type (143)
- Neoplasms, Nerve Tissue (143)
- Neoplastic Syndromes, Hereditary (143)
- Nervous System Diseases (143)
- Neurodegenerative Diseases (143)
- Genetic Diseases, Inborn (142)