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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.

12,578 public trials 2,158 recruiting studies

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Genetic Diseases, Inborn trial results

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Cascade Testing In Identifying At-risk Family Members Of Individuals With Familial Hypercholesterolemia (FH) In PCP

NCT07653555

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Hypercholesterolemia, +9 more
Locations: Mayo Clinic in Rochester Rochester, Minnesota, United States

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Patient Preferences in Treatment of Haemophilia A With and Without Inhibitors: a Discrete Choice Experiment in Germany

NCT07653139

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
Locations: Novo Nordisk Investigational Site Mainz, Gonsenheim, Germany

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Cryo-FIRST: Effectiveness of INTERCEPT Fibrinogen Complex (IFC) for Trauma-Associated Hemorrhage

NCT07218185

Conditions: Afibrinogenemia, Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, +15 more
Locations: Anschutz Medical Center, University of Colorado Aurora, Colorado, United States

Ryder Trauma Center/Jackson Memorial Hospital, University of Miami Miami, Florida, United States

R Adams Cowley Shock Trauma Center, University of Maryland Baltimore, Maryland, United States

Barnes Jewish Hospital, Washington University of Saint Louis St Louis, Missouri, United States

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Prospective Multicentre Observational Registry of Peri-procedural Anaesthesia, Sedation and Related Medication Exposure in Patients With Brugada Syndrome

NCT07655102

Conditions: Anesthesia, Arrhythmias, Cardiac, Brugada Syndrome, +10 more
Locations: Hospital Clinic de Barcelona Barcelona, Spain

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Biological Collection of the Rare Diseases of the Brain and Eye Vessels Cohort - 2

NCT07650110

Conditions: Brain Diseases, Brain Infarction, Brain Ischemia, +38 more
Locations: Not specified

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Prevalence of Cardiac Thrombi in Cardiac Amyloidosis

NCT07648303

Conditions: Amyloid Neuropathies, Amyloid Neuropathies, Familial, Amyloidosis, +13 more
Locations: Chu Dijon Bourogne Dijon, France

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Observational Study of Natural History of BAG3 Gene Mutation-Associated Dilated Cardiomyopathy in Chinese Adults

NCT07646600

Conditions: Cardiomegaly, Cardiomyopathies, Cardiomyopathy, Dilated, +6 more
Locations: Research Site Beijing, China

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FOsfomycin for Male Urinary Tract Infection

NCT06822751

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystitis, Endocrine Gland Neoplasms, +21 more
Locations: ELBEUF Elbeuf, France

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AI-based Echocardiography for Detection of Cardiac Amyloidosis

NCT07529860

Conditions: Amyloid Neuropathies, Amyloid Neuropathies, Familial, Amyloidosis, +24 more
Locations: Not specified

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Glucagon-Like Peptide-1 Receptor Agonists to Attenuate Metabolic Risk in Individuals With Duchenne Muscular Dystrophy

NCT07642635

Conditions: Body Weight, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +16 more
Locations: Vanderbilt University Medical Center Nashville, Tennessee, United States

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Genetic Diseases, Inborn

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