Rotator cuff tear Rotator cuff, shoulder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Aged 20 and over 2. Patients who were diagnosed with a rotator cuff tear 3. Patients who have an arthroscopic rotator cuff repair 4. Patients who have written consent to participate in this study
Exclusion criteria
Exclusion criteria: 1. Blood disorders, coagulation disorders or anticoagulants 2. Thrombosis 3. Malignancy 4. Acute inflammation 5. Polyneuropathy 6. Patients with skin disease in the irradiated area 7. Patients on long term cortisone therapy for more than 6 months or less than 6 weeks after the last cortisone injection 8. Pregnancy 9. Patients with contraindications to MRI 10. Patients using implantable defibrillators or pacemakers 11. Patients judged by the doctor to be unsuitable for inclusion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of retear by MRI findings | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Evaluation of pain Numerical Rating Scale (NRS) Consumption of analgesics Central Sensitization Inventory (CSI) Pain Detect 2) Evaluation of function Japanese Orthopaedic Association (JOA) score ASES score Constant score Range of motion Muscle strength DASH (Disability of the Arm, Shoulder, and Hand) 3) Evaluation of QOL SF-36v2 4) Evaluation of psychology HADS (Hospital Anxiety and Depression Scale) 5) MRI findings Sugaya classification Cuff repair integrity score Goutallier classification 6) Adverse event | — |
Contacts
Gunma University Hospital