The effect of Duloxetine on shoulder pain of patients with myofascial pain syndrome who undergo arthroscopic rotator cuff repair or adhesive capsulitis patient with glenohumeral injectio
- Conditions
- Diseases of the musculo-skeletal system and connective tissue
- Registration Number
- KCT0004361
- Lead Sponsor
- The Catholic University of Korea, Seoul St. Mary's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 76
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
? 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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS pain score
- Secondary Outcome Measures
Name Time Method 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