NCT06840717
- Conditions
- Asthma in Children, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, +6 more
- Locations
-
- Guangzhou institute of respiratory disease Guangzhou, Guangdong, China
Clinical trial condition
Genetic Disease
Explore clinical trials studying Genetic Disease. Study availability and eligibility vary by location and protocol.
89 public trials
37 recruiting studies
Genetic Disease trial results
NCT06821386
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Critical Care, Intensive Care, Genetic Disease, +3 more
- Locations
-
- National Taiwan University Hospital Taipei, Taiwan
NCT06775561
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Genetic Disease, +3 more
- Locations
-
- IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna, Italy
NCT06023472
- Conditions
- Aneuploidy, Chromosomal Rearrangement, Chromosome Aberrations, +8 more
- Locations
-
- Department of Obstetrics and Gynaecology Hong Kong, China
NCT03624374
- Conditions
- Ataxia, Ataxia, Cerebellar, Brain Diseases, +15 more
- Locations
-
- Hugo Moser Center for Leukodystrophies Baltimore, Maryland, United States
NCT06306521
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Disease, Genetic Diseases, Inborn
- Locations
-
- Rady Children's Hospital San Diego San Diego, California, United States
NCT04682470
- Conditions
- Cancer, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Distress, Emotional, +11 more
- Locations
-
- Antoni van Leeuwenhoekziekenhuis Amsterdam, North Holland, Netherlands
Not yet recruiting
Implementation-effectiveness Trial of Mainstreaming of Clinical Genomic Sequencing for Rare Disease in Ontario, Canada
NCT07799792
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Evaluation of Mainstreamed Models of Genetic Service Delivery, +6 more
- Locations
-
Not specified
Not yet recruiting
Multicenter Study of Patients With SHANK3 Mutations: Identification of Genes Modificators in Phelan-McDermid Syndrome (EUQ13)
NCT07119606
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Disease, Genetic Diseases, Inborn
- Locations
-
- Robert Debré Hospital Paris, Ap-hp / DRCI, France
Not yet recruiting
Rehabilitation Program on Genetic and Degenerative Ataxia
NCT06089863
- Conditions
- Ataxia, Brain Diseases, Central Nervous System Diseases, +11 more
- Locations
-
- Service de Rééducation Fonctionnelle (S.S.R.) Val Rosay Saint-Didier-au-Mont-d'Or, France
- Service de Médecine Physique et Réadaptation (M.P.R) de l'Hôpital Bellevue Saint-Etienne, France
- Service de Rééducation Fonctionnelle (S.S.R.) de l'Hôpital Henry Gabrielle Hospices Civils de Lyon Saint-Genis-Laval, France