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Genetic Disease

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Genetic Disease

Explore clinical trials studying Genetic Disease. Study availability and eligibility vary by location and protocol.

88 public trials 38 recruiting studies

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Genetic Disease trial results

Completed

Ensuring Patients' Informed Access to Noninvasive Prenatal Testing

NCT03420274

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Genetic Disease, +6 more
Locations: MetroHealth Medical Center Cleveland, Ohio, United States

Cleveland Clinic Cleveland, Ohio, United States

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Completed

Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders

NCT04399694

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Disease, +8 more
Locations: Duke University Durham, North Carolina, United States

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Completed

Fluoxetine in KCNC1-related Disorder

NCT06341127

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Disease, +5 more
Locations: Holland Bloorview Kids Rehabilitation Hospital Toronto, Ontario, Canada

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Completed

North Carolina Genomic Evaluation by Next-generation Exome Sequencing, 2

NCT03548779

Conditions: Autism Spectrum Disorder, Brain Diseases, Brain Malformation, +55 more
Locations: Mission Health Asheville, North Carolina, United States

University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States

East Carolina University Greenville, North Carolina, United States

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Completed

Technology Development for Noninvasive Prenatal Genetic Diagnosis Using Whole Fetal Cells From Maternal Peripheral Blood

NCT04285814

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Copy Number Abnormality, Genetic Disease, +2 more
Locations: Columbia University New York, United States

Baylor College of Medicine Houston, Texas, United States

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Completed

Newborn Genomic Sequencing Pilot Study

NCT06276348

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

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Completed

Genetic Screening and Assisted Oocyte Activation in Couples with Diminished/aberrant Embryonic Development.

NCT03354013

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Embryo, Embryo Disorder, +2 more
Locations: Ghent University Hospital Ghent, East-Flandres, Belgium

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Completed

A Comprehensive Approach To Relief Of Digestive Symptoms In Cystic Fibrosis: CARDS-CF

NCT05251467

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Disease, +8 more
Locations: Nottingham University Hospitals NHS Trust Nottingham, United Kingdom

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Completed

A Study to Evaluate DCR-PHXC in Children and Adults With Primary Hyperoxaluria Type 1 and Primary Hyperoxaluria Type 2

NCT03847909

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +16 more
Locations: Clinical Trial Site San Francisco, California, United States

Clinical Trial Site Boston, Massachusetts, United States

Clinical Trial Site Rochester, Minnesota, United States

Clinical Trial Site New York, United States

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Completed

Use of Long Read Genome Sequencing in Patients Suffering From Neurodevelopmental Troubles

NCT05643274

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Developmental Delay Disorder, Developmental Disabilities, +10 more
Locations: Brest University Hospital Brest, Finistère, France

Rennes University Hospital Rennes, Ille-et-Vilaine, France

Tours University Hospital Tours, Indre-et-Loire, France

Nantes University Hospital Nantes, Loire-Atlantique, France

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