Comparison of continuous interscalene block and continuous suprascapular nerve block
Not Applicable
Completed
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0005500
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
* rotator cuff tear patient scheduled to undergo arthroscopic rotator cuff repair
* American society of anesthesiologists physical status I/II/III
Exclusion Criteria
* patient who refuse to participate in this study
* patient with moderate/severe pulmonary disease
* patient with uncontrolled medical/psychological disease
* patient with trauma history on ipsilateral side
* patient with cervical disease, neuropathy, or myelopathy
* patient who requires additional open surgery
* patient who are contraindicated to NSAIDs, opioid, or ropivacaine
* female who is pregnant or lactating
* patient who are considered inappropriate by medical staffs due to other reasons
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method postoperative pain score
- Secondary Outcome Measures
Name Time Method the change of diaphragmatic excursion measured by ultrasound;Forced expiratory volume 1;postoperative opioid consumption;postoperative complications including hematoma, dyspnea