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ltrasound-guided suprascapular nerve block for postoperative pain control of rotator cuff repair : Proximal vs Distal approach

Not Applicable
Recruiting
Conditions
Diseases of the musculoskeletal system and connective tissue
Registration Number
KCT0006498
Lead Sponsor
Eulji University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
54
Inclusion Criteria

1) Adult patient of 18 years or older with a surgical indication of rotator cuff repair
1-1) Indication: A patient who clinically shows shoulder pain and reduction in function, and who has been diagnosed with the above-mentioned target disease in both physical and imaging examinations, requiring surgery
2) A patient who voluntarily agrees to the clinical trial and does not fall under the exclusion criteria
3) A patient who has been hospitalized for 3 or more days after surgery

Exclusion Criteria

1) Under 18 years of age
2) Acute fracture or aftereffect of a previous fracture
3) Acute or chronic infection around the shoulder joint
4) Patient with neurological dysfunction, including axillary nerve damage
5) Patient who is medically incapable of consent due to language or cognitive impairment
6) Immunosuppressed patient
7) Patient with mental illness who may affect follow-up results and rehabilitation
8) Patient who is addicted to drugs or other medications

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Regarding postoperative pain, the visual analogue scale for pain (VAS) score is observed
Secondary Outcome Measures
NameTimeMethod
The amount of narcotic analgesics used for postoperative pain control is observed by converting into MME (morphine milligram equivalent).
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