The goal of this clinical trial is to learn whether pretreatment central sensitization presence affect shoulder steroid injection resuls in patients with rotator cuff pathology. The main questions it aims to answer are: 1. Is central sensitization associated with decreased treatment response? 2. Do the clinical features of patients with central sensitization differ from those of those without? Participants will be applied a shoulder injection and the treatment response will be monitored.
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Visual analog scale
Timeframe: 1 week
Visual analog scale
Timeframe: 1 months
Visual analog scale
Timeframe: 3 months
Shoulder range of motion
Timeframe: 1 weeks
Shoulder range of motion
Timeframe: 1 months
Shoulder range of motion
Timeframe: 3 months