The Role of Muscle Ultrasound in Assessment of Sample of Patients With Limb-girdle Muscular Dystrophy
1 other identifier
observational
50
0 countries
N/A
Brief Summary
- 1.to detect the characteristic patterns of muscle involvement in suspected cases of LGMD using muscle ultrasound
- 2.to use the muscle ultrasound findings clinically categorized the different types of LGMD
- 3.to correlate the muscle ultrasound findings with the findings of the other assissed scales
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2024
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 1, 2024
CompletedFirst Posted
Study publicly available on registry
May 6, 2024
CompletedStudy Start
First participant enrolled
June 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
May 6, 2024
May 1, 2024
2 years
May 1, 2024
May 1, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
The role of muscle ultrasound in assessment of a sample of patients with limb-girdle muscular dystrophy
The role of muscle ultrasound in assessment of sample of patients with LGMD
Baseline
Interventions
Role of muscle ultrasound in LGMD
Eligibility Criteria
* Patients presented with clinical manifestations suggestive of LGMD who presented with gradual progressive limb-girdle weakness ,myopathic changes on electromyography and elevated creatine phosphokinase serum level * age and sex matched healthy control group as a normal referencce
You may qualify if:
- gender : both sex are included Willingness to participate in the study and to be subjected to disease related examination and assessments Willing and able to provide informd consent
You may not qualify if:
- patients unable to give informed consent Patients with acute or subacute onset of symptoms of muscle involvement including inflammatory myopathies Patients with systemic diseases causing secondary myopathy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Abanoub bassem
Study Record Dates
First Submitted
May 1, 2024
First Posted
May 6, 2024
Study Start
June 1, 2024
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
July 1, 2026
Last Updated
May 6, 2024
Record last verified: 2024-05