Comprehensive Study of Duchenne Muscular Dystrophy at Sohag University Hospital

Sohag University

Status: Unknown

Conditions: Duchenne Muscular Dystrophy

Treatments: Diagnostic Test: MLPA for duchenne

Study type: Interventional

Funder types: Other

Identifiers

NCT05029232

Soh-Med-21-07-21

Details and patient eligibility

About

Muscular dystrophies are a heterogenous group of inherited muscular disorders characterized by progressive muscle weakness. Historically, these disorders are difficult to treat. In the last three decades, there is a great progress in molecular and genetic basis of these disorders; early diagnosis is achievable with proper clinical recognition and advanced genetic testing .Duchenne Muscular Dystrophy (DMD) is a neuromuscular muscular X-linked recessive disorders that belong to a group of disorders known as dystrophinopathies. DMD characterized by a progressive degeneration of skeletal muscles, with symptoms that manifest early, at around 3 years, causing loss of ambulation within the 13 years of life, followed by cardiac complication (e.g., dilated cardiomyopathy and arrhythmia) and respiratory disorders, including chronic respiratory failure. The unique medical treatment available is steroid therapy, which appears to prolong walking capacity by at least two years. Thus, besides medical treatment, the physical therapy in multidisciplinary care is imperative for alleviating muscle atrophy, skeletal deformities, and motor function deterioration.

Enrollment: 50 estimated patients

Sex: Male

Ages: 3 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. age of onset between 3- and 18-year-old
2. typical clinical manifestation of Duchenne muscular dystrophy
3. clinical manifestation confirmed by specific biochemical analysis or by genetic testing who presented to pediatric department and neurology outpatient clinic during the period of study.

Exclusion criteria

1. children with another congenital muscular dystrophy
2. children with other types of myopathies
3. presence of CNS disorders such as brain insult & spinal muscular atrophy
4. female gender

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

ambulant patient with DMD

Active Comparator group

Description:

patient that walk alone or with minor assist

Treatment:

Diagnostic Test: MLPA for duchenne

non ambulant patient with DMD

Active Comparator group

Description:

patient need wheel chair

Treatment:

Diagnostic Test: MLPA for duchenne