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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.

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Genetic Diseases, Inborn trial results

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Multimodal Radiomics Model (18F-FAPI PET/CT + CMR) for AL Cardiac Amyloidosis Prognosis

NCT07103863

Conditions: AL Amyloidosis (AL), Amyloid Neuropathies, Amyloid Neuropathies, Familial, +22 more
Locations: Beijing Anzhen Hospital Beijing, Beijing Municipality, China

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Subthreshold Micropulse Laser Therapy (SML) in Retinitis Pigmentosa

NCT07088705

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +6 more
Locations: First Department of Ophthalmology, Pomeranian Medical University Szczecin, Poland

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Group Coaching Study for Life Goals

NCT07083713

Conditions: Cardiovascular Diseases, Care Givers, Central Nervous System Diseases, +23 more
Locations: Thomas Jefferson University Philadelphia, Pennsylvania, United States

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The Use of Assistive Gait Devices Can Reduce the Risk of Falls in Patients With Neuromuscular Diseases Following a Training Period.

NCT07072676

Conditions: Autoimmune Diseases, Autoimmune Diseases of the Nervous System, Brain Diseases, +69 more
Locations: Medical Park, Bad Feilnbach, Reithofpark Bad Feilnbach, Germany

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Long-term Follow-up Study of Male Adults With Hemophilia B Previously Treated With Etranacogene Dezaparvovec (CSL222)

NCT05962398

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
Locations: 10-15 Phoenix Childrens Hospital Phoenix, Arizona, United States

10-14 Arkansas Children's Hospital - Pharmacology Little Rock, Arkansas, United States

10-22 Orthopaedic Institute for Children Los Angeles, California, United States

10-21 Children's Hospital of Los Angeles Los Angeles, California, United States

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Prospective Exploratory Cohort Study on Ganglion Cell Degeneration in Retinitis Pigmentosa Patients

NCT07056738

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: EKFZ Else Kroener Fresenius Center for Optogenetic Therapies, University Medical Center Goettingen Göttingen, Germany

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Comparing Structured Neuromuscular Exercise and Exergaming Program in Adolescents With Familial Mediterranean Fever

NCT07013045

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Familial Mediterranean Fever, Familial Mediterranean Fever (FMF ), +2 more
Locations: Istanbul University-Cerrahpasa Istanbul, Turkey (Türkiye)

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Clinical Study to Evaluate the Efficacy and Safety of Matrix Pro Treatment

NCT06726122

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, Cutis Laxa, +7 more
Locations: Kliniek voor Esthetische Geneeskunde Amsterdam, EK, Netherlands

Illuminate Skin & Wellness Clinic Kings Hill, Kent, United Kingdom

GHB Clinic London, United Kingdom

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The Remote Monitoring of Gout Study

NCT06822933

Conditions: Arthritis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crystal Arthropathies, +10 more
Locations: Diakonhjemmet Hospital Oslo, Please Select, Norway

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Follow-up Study on Female Carriers With DMD Gene Variants

NCT05715957

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +10 more
Locations: Copenhagen neuromuscular center Copenhagen, Denmark

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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