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Clinical Trials/NL-OMON41430
NL-OMON41430
Completed
Not Applicable

SISTIM: Subacromial Impingement Syndrome: The Identification of etiologic Mechanisms will have a new acronym respectively, SuSy SuSy: Subacromial Impingement Syndrome: The Identification of etiologic Mechanisms - SISTIM, new acronym, SuSy

eids Universitair Medisch Centrum0 sites110 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
painful arc syndrome
Sponsor
eids Universitair Medisch Centrum
Enrollment
110
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • The clinical diagnosis of stage I or II SIS is made when one or more of the following mentioned factors exist, next to a positive Neer impingement test and a positive Hawkins test.;Patients\* history:
  • \- Diffuse unilateral shoulder pain for \> 3 months;
  • \- Pain during activities with abduction, retroflexion and/or internal rotation (i.e. closing the door, putting on jacket, overhead activities);
  • \- Pain at night or incapable of lying on the shoulder.;Physical examination:
  • \- Diffuse pain at palpation of the greater tuberosity;
  • \- Disturbed scapulohumeral rhythm;
  • \- Painful arc;
  • \- No complaints or sings of pathologies on the contralateral shoulder;
  • \- \> 90 Degrees external rotation in 90 degrees of passive abduction (frozen shoulder);
  • \- Positive Yocum test.

Exclusion Criteria

  • Patients are excluded if one of the following characteristics is found:
  • \- \<35 Or \> 60 years old
  • \- Restrictions in passive movements of glenohumeral joint/frozen shoulder;
  • \- History of fracture or dislocation of the shoulder;
  • \- History of surgery around the shoulder (in anamnesis);
  • \- No informed consent;
  • \- Clinical and radiographic signs of comorbidities or alternative diagnoses on the affected shoulder (glenohumeral instability, glenohumeral movement restriction, glenohumeral osteoarthritis or arthritis, rheumatic disorder, labrum lesions, a history of trauma on the affected shoulder, biceps muscle tendinitis, complete (full thickness) rotator cuff rupture, cervical radiculopathy, PASTA lesion, or calcifying tendinitis);
  • \- Contralateral shoulder with clinical signs of shoulder complaints.
  • \- Pacemaker or other electronic implants

Outcomes

Primary Outcomes

Not specified

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