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Genetic Diseases, Inborn

Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,656 public trials 2,147 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment: HABIT

NCT02029742

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +13 more
Locations: Columbia University Medical Center New York, United States

Montefiore Medical Center - Albert Einstein College of Medicine The Bronx, New York, United States

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Completed

Effects of Ondansetron in Obsessive-compulsive and Tic Disorders

NCT03239210

Conditions: Anxiety Disorders, Basal Ganglia Diseases, Brain Diseases, +12 more
Locations: New York University School of Medicine New York, United States

The Nathan S. Kline Institute for Psychiatric Research New York, United States

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Completed

Prader-Willi Syndrome Body Composition

NCT04597645

Conditions: Abnormalities, Multiple, Atrophy, Body Weight, +23 more
Locations: Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation New Taipei City, Taiwan

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Completed

Use of Partial Body Weight Support Play Environment to Encourage Mobility and Exploration in Infants With Down Syndrome

NCT05307523

Conditions: Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +8 more
Locations: Center on Human Development and Disability (CHDD) Seattle, Washington, United States

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Completed

PINPOINT: Gaming Technology for SCD Pain

NCT04579926

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +10 more
Locations: Klein Buendel, Inc. Golden, Colorado, United States

Hilton Publishing Company Munster, Indiana, United States

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Completed

Effect of Rate Of Delivery on Colonic Fermentation of inuliN (EON)

NCT05619341

Conditions: Carbohydrate Metabolism, Inborn Errors, Colonic Diseases, Colonic Diseases, Functional, +16 more
Locations: Nottingham Digestive Disease Centre Nottingham, Nottinghamshire, United Kingdom

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Completed

The Use of Novel Diagnostic Tools to Increase Detection of Early Fibrosis in Cystic Fibrosis Related Liver Disease to Improve Clinical Management

NCT04277819

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Cystic Fibrosis Liver Disease, +12 more
Locations: Wythenshawe Hospital Manchester, United Kingdom

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Completed

Smith-Lemli-Opitz Syndrome and Cholic Acid

NCT03720990

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: Colorado Children's Hospital Aurora, Colorado, United States

University of Nebraska Medical Center Omaha, Nebraska, United States

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Completed

Proton Pump Inhibitors (PPI) and Fat Absorption in Cystic Fibrosis (CF) and Exocrine Pancreatic Insufficiency (EPI)

NCT03551691

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +7 more
Locations: Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States

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Completed

Combined CBIT and rTMS to Improve Tourette's Syndrome

NCT04795908

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +10 more
Locations: Fixel Neurologic Institute Gainesville, Florida, United States

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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