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Muscular Dystrophies clinical trials

View clinical trials related to Muscular Dystrophies.

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NCT ID: NCT06379906 Completed - Clinical trials for Duchenne Muscular Dystrophy

Upper Extremity Muscle Strength, Balance and Functional Skills in DMD

Start date: November 10, 2023
Phase:
Study type: Observational [Patient Registry]

This study aims to examine the relationship between upper extremity muscle strength, balance and functional skills of children with DMD.

NCT ID: NCT06378203 Recruiting - Clinical trials for Muscular Dystrophies

Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project [RIMUDI]

RIMUDI
Start date: December 15, 2023
Phase: N/A
Study type: Interventional

Until twenty years ago physical exercise in muscular dystrophies was considered harmful to the muscle cells, inducing an acceleration of cell necrosis. In fact, it is now certain and validated that an active lifestyle and the practice of controlled and regular physical activity are to be considered therapeutic in neuromuscular pathologies with the aim of optimizing muscular and cardio-respiratory function and preventing atrophy In particular, it seems that the optimal care is extensive and can be carried out in a safe and controlled manner even at home. It is well documented that exercise has beneficial effects on muscle with increased strength and muscular endurance.

NCT ID: NCT06366815 Recruiting - Clinical trials for Duchenne Muscular Dystrophy

phenotypeS in Non Ambulant Duchenne Muscular Dystrophy

GUP21003
Start date: August 30, 2022
Phase:
Study type: Observational [Patient Registry]

The aims of the study are to prospectively collect information on several aspects of function in non-ambulant DMD patients by using a structured battery of tests including motor, respiratory and cardiac function

NCT ID: NCT06363526 Not yet recruiting - Clinical trials for Duchenne Muscular Dystrophy

Effectiveness of 5-week Digital Respiratory Practice in a Group of Children With Duchenne Muscular Dystrophy and Becker Muscular Dystrophy.

DMDrespy2024
Start date: May 5, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to analyze the effectiveness of a 5-weeks respiratory digital intervention program in patients with Duchenne muscular dystrophy and Becker muscular dystrophy.

NCT ID: NCT06363357 Recruiting - Clinical trials for Muscular Dystrophy, Duchenne

The Effect of a Muscle-mimicking, Fabric-type Shoulder Orthosis on Functional Movements of the Upper Limb in Patients With Duchenne Muscular Dystrophy

Start date: April 20, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate the effect of a muscle-mimicking, fabric-type shoulder orthosis on functional movements of the upper limb in patients with Duchenne muscular dystrophy. The main questions it aims to answer are: - What is the impact of the muscle-mimicking, fabric-type shoulder orthosis on upper limb functional movements in patients with Duchenne muscular dystrophy? - Are there observable differences in upper limb function when the shoulder orthosis is worn versus when it is not? Participants will: - Receive education on how to wear and use the shoulder orthosis. - Undergo evaluations, including assessment of upper limb performance, shoulder muscle strength testing, active range of motion measurements, assessment of functional workspace, goal attainment scale evaluation, surface electromyography, physiological measurements such as blood pressure and heart rate, fatigue assessment, and assessment for any musculoskeletal or skin-related issues. Researchers will compare Duchenne muscular dystrophy patients before and while wearing and operating the shoulder orthosis to see if there are any significant effects on variables such as upper limb function, range of motion, functional workspace, goal attainment scale, and surface electromyography.

NCT ID: NCT06354790 Not yet recruiting - Clinical trials for Merosin Deficient Congenital Muscular Dystrophy

Natural History Study of Children With LAMA2-related Dystrophies

LAMA2
Start date: June 15, 2024
Phase:
Study type: Observational

The goal of this natural history study is to characterize the disease course, characteristics in paediatric population of LAMA2-RD (related dystrophies) patients. The aim of the study is to establish a well-described cohort of patients in France with LAMA2-RD for prospective follow-up and recruitment for future clinical trials. Participants will be follow up during a two years period regarding exhaustive aspects of the pathology: - Muscular function - Respiratory function - Cognitive phenotyping - Quality of life - Growth parameters - Biomarkers

NCT ID: NCT06337669 Recruiting - Clinical trials for Muscular Dystrophy, Duchenne

Characterization of DupEx2 Duchenne Muscular Dystrophy

DMDDup2
Start date: January 31, 2022
Phase:
Study type: Observational

To characterize the clinical phenotype and possible predictive/prognostic factors of patients with Duchenne muscular dystrophy (DMD) due to duplication of exon 2 (Dup2). Specifically, we aim 1) to describe the progression of motor, respiratory and cardiac function; 2) to enquire if the phenotypic spectrum of Dup2 is milder than classic DMD, 3) to perform whole genome sequencing (WGS) to characterize DNA breakpoints to correlate with the phenotype; 4) to collect material for future proteomic/transcriptomic studies. Background/Rationale DMD is caused by mutations in the DMD gene and in 11% of cases is due to duplications. The most promising therapeutic approaches include mutation-specific therapies. Notably, there is increasing evidence that specific groups of mutations may underlie different disease trajectories compared to the "average" DMD population. It is thus mandatory to have more information on genotype-phenotype correlations and patterns of progression related to different genotypes. Dup2 is the most common DMD duplication and the only one for which a AAV-mediated exon skipping study is ongoing. Despite most case series and databases ascribe Dup2 to severe phenotype, our preliminary findings sustain that these patients have collectively a milder progression of the disease and in 1/3 of cases a significantly milder phenotype. Moreover, our attempts to reveal mechanism involved in attenuating the phenotype would confute the hypothesis of alternative spicing transcripts as previously described for DMD with deletion of exon 2. Research design and methods Clinical information regarding a cohort of 26 Italian Dup2 patients will be collected. Differences in time to loss of ambulation compared to a DMD control group will be achieved. Finally, we will retrieve DNA for correlative WGS studies. Anticipated output We expect that Dup2 patients present a milder DMD phenotype , which might be predicted by genomic studies.

NCT ID: NCT06328725 Not yet recruiting - Clinical trials for Duchenne Muscular Dystrophy

Evaluate the Efficacy and Safety of EN001 in Patients With Duchenne Muscular Dystrophy

Start date: March 2024
Phase: Phase 1/Phase 2
Study type: Interventional

A Multi-center, Randomized, Double-blind, Placebo-controlled, Phase 1/2 Trial to Evaluate the Efficacy and Safety of EN001 in Patients with Duchenne Muscular Dystrophy

NCT ID: NCT06304064 Completed - Clinical trials for Duchenne Muscular Dystrophy

Halt cardiomyOPathy progrEssion in Duchenne (HOPE-OLE)

HOPE-OLE
Start date: June 21, 2018
Phase: Phase 2
Study type: Interventional

This Phase 2, multi-center, open-label extension trial will provide CAP-1002 to participants who were randomized to the Usual Care treatment group of the HOPE-Duchenne study (NCT02485938) and completed 12 months of follow-up. The trial will assess the safety and efficacy of two intravenous administrations of CAP-1002, each separated by three months.

NCT ID: NCT06295718 Enrolling by invitation - Clinical trials for Duchenne Muscular Dystrophy

Tele-assessment of Functional Performance and Quality of Life in Patients With Duchenne Muscular Dystrophy: Validity and Reliability Study

Start date: July 1, 2023
Phase:
Study type: Observational

Thanks to tele-assessment methods, it may be possible to evaluate DMD patients without traveling to clinical centers. In recent years, the applicability of remote assessment methods in DMD patients, as in many populations, is being investigated. However, studies have generally focused on a single evaluation parameter such as physical function, a special evaluation method or a special evaluation tool. The aim of this study is to investigate whether remote assessment of functional performance and quality of life in DMD patients is valid and reliable. If a valid and reliable tele-evaluation method that includes functional performance and quality of life parameters is found to be valid and reliable, the travel burden on patients and caregivers can be eased, patients' stress and anxiety related to travel can be reduced, caregivers can save time and energy and provide patients with the best possible treatment.