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Genetic Diseases, X-Linked

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Genetic Diseases, X-Linked

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

1,243 public trials 227 recruiting studies

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Genetic Diseases, X-Linked trial results

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Validity and Reliability of the Two-minute Step Test in Hemophilia

NCT07425327

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +11 more
Locations: Hasan Kalyoncu University Gaziantep, Şahinbey, Turkey (Türkiye)

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An Open-label, Phase 2 Pilot Study on the Efficacy and Safety of Piclidenoson in Patients With Lowe Syndrome

NCT07410455

Conditions: Abnormalities, Multiple, Amino Acid Transport Disorders, Inborn, Brain Diseases, +20 more
Locations: IRCCS Ospedale Pediatrico Bambino Gesù Roma, Italy

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Registry for Duchenne and Becker Muscular Dystrophy

NCT07402122

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Universitätsklinikum Essen Klinik für Kinderheilkunde I Essen, Germany

Universitätsklinik Heidelberg, Zentrum für Kinder- und Jugendmedizin Heidelberg, Germany

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Factors Influencing Physical Activity Levels in Children With Duchenne Muscular Dystrophy: An ICF-CY-Based Study

NCT07369609

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Not specified

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DMD and Gamified Physiotherapy

NCT07368400

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Not specified

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Self-Efficacy Enhancement Using a Multicomponent Support Group for Caregivers of Children With DMD/SMA

NCT07356063

Conditions: Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +14 more
Locations: Not specified

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Novel Diagnostic and Prognostic Predictors in Fabry Cardiomyopathy: Proof of Concept in a Rare Disease

NCT07351136

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Not specified

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Inhibition of Aggressive Behavior in Participants With Fragile X Syndrome

NCT07328529

Conditions: Aberrant Motor Behavior in Dementia, Aggression, Aggressive Behavior in Fragile X Syndome, +22 more
Locations: University of California, Davis, MIND Institute Sacramento, California, United States

Rush University Medical Center Chicago, Illinois, United States

Cincinnati Children's Hospital Cincinnati, Ohio, United States

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Efficacy and Safety of NTI164 in Children and Young Adults With Rett Syndrome

NCT07257978

Conditions: Chemically-Induced Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
Locations: Monash Health Clayton, Victoria, Australia

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Epiretinal Membrane in Patients With DR.

NCT07241845

Conditions: Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +14 more
Locations: Not specified

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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