Ultrasound Detection of Early Facial Muscle Changes in FSHD: Thickness and Echo Intensity Findings
NCT ID: NCT07331025
Last Updated: 2026-01-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
39 participants
OBSERVATIONAL
2023-09-01
2024-02-15
Brief Summary
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The aim of this study is to compare facial muscle thickness and echo density between FSHD patients and healthy controls using ultrasound and to examine the relationships between ultrasound findings and clinical parameters.
This study will include 20 patients with genetically confirmed FSHD1 diagnosis and 19 age- and sex-matched healthy controls. Using musculoskeletal ultrasound, bilateral evaluation of selected facial muscles (Orbicularis oculi, orbicularis oris, zygomaticus major, and buccinator) will be performed by two different researchers, and muscle thickness and muscle echo density will be recorded. Inter-rater reliability will be assessed using intraclass correlation coefficients. Group comparisons and correlation analyses will be performed with clinical scores, symptom duration, and D4Z4 repeat size.
The results will evaluate whether ultrasound can reliably detect structural changes in FSHD that cannot be captured by traditional clinical assessments, and if significant, will suggest that ultrasound can serve as a sensitive imaging biomarker for early and region-specific facial muscle involvement in FSHD.
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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FSHD patients
Individuals with genetically confirmed facioscapulohumeral muscular dystrophy type 1 who underwent bilateral facial muscle ultrasound assessment. No intervention was applied.
No interventions assigned to this group
Healthy Controls
Age- and sex-matched healthy volunteers without neuromuscular disease.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Genetically confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) (patient group)
* Age- and sex-matched healthy volunteers without neuromuscular disease (control group)
* Ability to provide written informed consent
Exclusion Criteria
* History of facial palsy or facial trauma
* Botulinum toxin injection to facial muscles within the last 6 months
* Inability to cooperate with ultrasound assessment
18 Years
55 Years
ALL
Yes
Sponsors
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Koç University
OTHER
Responsible Party
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Havvanur Albayrak
Physical Medicine and Rehabilitation Specialist
Principal Investigators
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Havvanur Albayrak
Role: PRINCIPAL_INVESTIGATOR
Koç University School of Medicine
Locations
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Koç University Hospital
Istanbul, Istanbul, Turkey (Türkiye)
Countries
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Other Identifiers
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2023.278.IRB1.092
Identifier Type: OTHER
Identifier Source: secondary_id
2023.278.IRB1.092
Identifier Type: -
Identifier Source: org_study_id
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