Rotator cuff injury
Conditions
Interventions
Test group:Analgesia is relieved by buprenorphine transdermal patches after surgery for rotator cuff injuries
Control group:Acromikates are followed by a nonsteroidal anti-inflammatory drug combined with tramadol analgesia
Sponsors
Drum Tower Hospital Affiliated to Nanjing University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Pain in the shoulder during rest or movement (2) MRI shows partial damage to the rotator cuff (3) Partial injury to the rotator cuff is indicated by surgery
Exclusion criteria
Exclusion criteria: (1) The age of the patient 70 years old (2) There are other local or systemic diseases that affect the function of the shoulder joint (3) There is a history of rotator sleeve repair (4) There is a tear that requires open repair or open biceps tendon fixation (5) Asthma, urticaria or, or after taking aspirin or other NSAIDs Patients with allergic reactions (6) Transdermal patches known or suspected for tramadol, celecoxib capsules, and buprenorphine Agents, acetaminophen and their excipients have a history of allergy and serious adverse reactions (7) Dicoumarin anticoagulants (warfarin, etc.), methotrexate, lithium are being used Agents, thiazide diuretics (hydrochlorothiazide), loop diuretics (furosemide). (8) After surgery, use continuous epidural analgesia, intravenous analgesic pump, and local closed town People with pain, or those who use other pain relief measures (9) Heart bypass suffers (10) The latter is performed before coronary artery bypass grafting (11) Peptic ulcer patients or those with a history of peptic ulcer (12) A history of gastrointestinal bleeding or perforation after previous use of NSAIDs he who (13) Patients who exhibit allergic reactions to sulfonamides (14) Users of antidepressants (15) Opioid dependent (16) Hemodynamically unstable and morbidly obese (17) Severe liver and kidney damage (18) Pregnant or lactating women (19) Severe heart failure (20) Any other researcher who deems it unsuitable for inclusion in the study or completion of the study factor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual simulation scale;American Shoulder Elbow Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| The number and number of people used to rescue drugs;Sleep disturbances; | — |
Countries
China
Contacts
Public ContactJiangHui Qin
Drum Tower Hospital Affiliated to Nanjing University School of Medicine
Outcome results
None listed