shoulder tendinopathy
Not Applicable
- Conditions
- M25.51
- Registration Number
- DRKS00011054
- Lead Sponsor
- Klinik für Orthopädie und Unfallchirurgie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 88
Inclusion Criteria
•Symptomatic rotator cuff tendinopathy
•At least a 3-month duration of symptoms
•Must complete and failed to conservative treatment with:
oPhysical therapy and
ophysiotherapy
oSystemic NSAID´s
•NSAIDs treatment washout period of 1 weeks
•No calcific tendinitis
•Signed informed consent
•VAS pain score > 4
•Age greater than 18 years
Exclusion Criteria
•Glenohumeral or acromioclavicular joint arthrosis
•Previous surgery of the painful shoulder
•Bursitis/ infection/ tumor of the shoulder
•Shoulder Instability/ clinically significant complete rotator cuff lesion of the shoulder
•Pathological neurological findings
•VAS Pain score < 5
•Significant coagulation disturbance
•Previous unsuccessful ESWT
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method shoulder pain measured by visual analogue scale (VAS) 6, 12 and 24 month after last intervention
- Secondary Outcome Measures
Name Time Method funcunal outcome of the painful shoulder measured by Constant Murley Score (CMS) 6, 12 and 24 month after last intervention