None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion Criteria ? Patients diagnosed with myofascial pain syndrome who are over 19 years old and younger than 70 years who underwent arthroscopic rotator cuff repair due to complete rotator cuff tear ? Patients with central sensitization (Central Sensitization Inventory (CSI) score of 40 or more) ? Patients who understand this study and agree to participate in the study
Exclusion criteria
Exclusion criteria: Exclusion Criteria ? Non-central sensitization patients (Central Sensitization Inventory (CSI) score below 40) ? Patients who have previously taken Duloxetine ? Patients with hypersensitivity or excessive complications after taking Duloxetine ? Patients diagnosed and treated for psychiatric disease ? Patients with local infection, sepsis, or previous neurological abnormalities ? Patients with uncontrolled hypertension who have more than 100mmHg of diastolic blood pressure ? Patients with abnormal liver function (aspartate aminotransferase or alanine aminotransferase> 60 IU litre) ? Patients with severe cardiovascular disease or kidney disorders
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Shoulder joint range of motion;Functional scores (ASES score, Constant score, KSES score);Mental component summary score of the Short Form-36 (SF-36) II, Hamilton depression scale | — |
Primary
| Measure | Time frame |
|---|---|
| VAS pain score | — |
Countries
Korea, Republic of
Contacts
The Catholic University of Korea, Seoul St. Mary's Hospital