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Genetic Diseases, Inborn

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Genetic Diseases, Inborn

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

12,633 public trials 2,161 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

Imaging Cardiac Amyloidosis: A Pilot Study Using F-18 Florbetapir Positron Emission Tomography

NCT01683825

Conditions: Amyloid Neuropathies, Amyloid Neuropathies, Familial, Amyloidosis, +16 more
Locations: Brigham and Women's Hospital Boston, Massachusetts, United States

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Completed

6 Minute Walk Test in Cystic Fibrosis

NCT02538575

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: Hôpital Cochin, service de pneumologie Paris, France

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Completed

Allergic Disease Onset Prevention Study

NCT05003804

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +10 more
Locations: University of Arizona Health Sciences Tucson, Arizona, United States

Arkansas Children's Research Institute Little Rock, Arkansas, United States

UCLA Health Los Angeles, California, United States

Rady Children's Hospital - San Diego San Diego, California, United States

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Completed

Development of a New Tool for Dyspnea Measurement in Chronic Respiratory Diseases

NCT02229994

Conditions: COPD (With - Without Rehabilitation), Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +24 more
Locations: Service de Pneumologie AP-HP, Hôpitaux Universitaires Paris Centre Paris, France

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Completed

Parenting Concerns in Patients With Cystic Fibrosis (MucoPar)

NCT04133246

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: Cochin Hospital Paris, Île-de-France Region, France

Foch Hospital Suresnes, Île-de-France Region, France

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Completed

Imaging Study of the White Matter Lesions in Children With Metachromatic Leucodystrophy

NCT01325025

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Unité de recherche biomédicale, Neurospin, I2BM / DSV / SAC/ CEA, Gif-sur-Yvette, France

Service de Neurologie Pédiatrique, Hôpital Bicêtre Paris, France

Bâtiment Lavoisier - Unité INSERM U 663,Hôpital Necker Enfants Malades Paris, France

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Completed

Concerns of Children Whose Parents Have Cystic Fibrosis

NCT04702386

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: Cochin Hospital Paris, France

Foch Hospital Suresnes, France

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Completed

Impact of Global Care of the Pain at Chronic Painful Patients Affected by Cystic Fibrosis

NCT01915875

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: hôpital Necker Enfants malades Paris, France

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Completed

Study of the Pathophysiological Mechanisms Involved in Bleeding Events

NCT01314560

Conditions: Abnormalities, Multiple, Amino Acid Transport Disorders, Inborn, Brain Diseases, +25 more
Locations: Necker Enfants Malades Hospital, Genetic Paris, France

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Completed

Comparison of Non-invasive Measurement Methods of Hepatic Fibrosis in Cystic Fibrosis

NCT02342964

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +10 more
Locations: Hôpital Necker Paris, France

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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