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Muscular Dystrophies

Clinical trial condition

Muscular Dystrophies

Explore clinical trials studying Muscular Dystrophies. Study availability and eligibility vary by location and protocol.

452 public trials 90 recruiting studies

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Muscular Dystrophies trial results

Completed

Frailty Scales for Predicting Chemotherapy Toxicity in Older Adults With Gastrointestinal Cancers

NCT07184047

Conditions: Atrophy, Biliary Tract Cancer, Biliary Tract Diseases, +53 more
Locations: Etlik City Hospital, Medical Oncology Department Ankara, Yenimahalle, Turkey (Türkiye)

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Completed

An Open-label, Multidose Dose-escalation Study to Understand the Safety of CRISPR Gene-editing Therapy and Its Long-Lasting Effects in DMD Patients (MUSCLE)

NCT06594094

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophin (DMD), Genetic Diseases, Inborn, +8 more
Locations: Shanghai Children s Medical Center Affiliated to Shanghai Jiao Tong University School of Medical Shanghai, Shanghai Municipality, China

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Completed

A Trial to Investigate Safety and Pharmacokinetics of GRT6019, Including Food Effect, in Healthy Male Participants

NCT07317063

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +8 more
Locations: Biotrial, Inc Newark, New Jersey, United States

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Completed

Longitudinal Evaluation of Neuromuscular Involvement in Type 1 Myotonic Dystrophy

NCT07362316

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: Centre de recherche du CHU de Québec-Université Laval Laval, Canada

Institut de Myologie Paris, Île-de-France Region, France

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Completed

Virtual Reality and Whole Body Vibration on Muscle Strength and Balance in Children With DMD

NCT07338812

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +8 more
Locations: Cairo university Cairo, Egypt

Cairo university Giza, Egypt

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Completed

Ultrasound Detection of Early Facial Muscle Changes in FSHD: Thickness and Echo Intensity Findings

NCT07331025

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy 1, +9 more
Locations: Koç University Hospital Istanbul, Turkey (Türkiye)

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Completed

Factors Associated With Hypoventilation in the Myotonic Dystrophy, Progressive Profile Over 5 Years

NCT03764150

Conditions: Apnea, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyssomnias, +17 more
Locations: Centre Hospitalier Regional D' Angers Angers, France

Ap-Hp Hu Paris Site Raymond Poincare Garches, France

Hôpital Calmette, CHRU Lille, France

Chu Montpellier Montpellier, France

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Completed

Nutritional Status and Therapy in DMD Patients

NCT06682585

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +8 more
Locations: DMD Aileleri Derneği Ankara, Çankaya, Turkey (Türkiye)

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Completed

Nebivolol for the Prevention of Left Ventricular Systolic Dysfunction in Patients With Duchenne Muscular Dystrophy

NCT01648634

Conditions: Cardiomyopathies, Cardiomyopathy, Cardiovascular Diseases, +13 more
Locations: Armand Trousseau Hospital Paris, France

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Completed

Study of SRP-4045 (Casimersen) and SRP-4053 (Golodirsen) in Participants With Duchenne Muscular Dystrophy (DMD)

NCT02500381

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Neuromuscular Research Center Phoenix, Arizona, United States

Children's Hospital Los Angeles Los Angeles, California, United States

David Geffen School of Medicine, UCLA Los Angeles, California, United States

Rady Children's Hospital San Diego/ UCSD San Diego, California, United States

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