About this trial
This study is a prospective blind study of periscapular muscle thickness measured with MSUS and correlate it with EMG findings.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The inclusion criterion for the first group is patients with SD with inflammatory characteristics.
The inclusion criterion for the second group is patients complaining of discomfort upon activity.
Disqualifiers
patients with a history of local trauma
patients with surgical intervention,
neuromascular deficits,
chronic chest disease
Trial population
* The first group: patients with SD with inflammatory characteristics. * The second group: patients with SD complaining of discomfort upon activity.
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
periscapular muscle thickness measured with MSUS in all patients
Measurement of periscapular muscle thickness with MSUS in all patients and to correlate it with EMG findings.
Sponsors and contacts
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