Analgesic efficacy comparison after arthroscopic rotator cuff repair : continuous arthroscopically assisted suprascapular nerve block versus ultrasound-guided continuous inter-scalene block

Not Applicable

Recruiting

• Conditions: Diseases of the musculo-skeletal system and connective tissue

• Registration Number: KCT0004800
• Lead Sponsor: Asan Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 23 March 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 76

Inclusion Criteria

1. Patients over 50 years old and under 80 years old
2. Arthroscopic Rotator Cuff Repair
3. Rotator cuff tear
4. Suture Result after Surgery: Type I ~ II (Complete repair)
5. Size of rupture: small, small to medium, medium to large
6.Repair method: Single row or Double row suture bridge technique
7. Patients with an ASA score I / II / III
8. The patient has consented to the operation and procedure.

Exclusion Criteria

1.BMI> 30 kg / m2
2. Patients with a psychiatric history.
3. Patients with other respiratory diseases such as COPD
4. Patients with previous trauma to the lesion
5. Patients with cervical disease and neuropathy
6. Patients with coagulation or taking anticoagulant drugs.
7. Patients with myopathy
8. Patients in need of additional incision surgery in addition to arthroscopic surgery.
9. Infectious diseases, degenerative diseases, rheumatoid arthritis
10. Stroke, gastritis or gastric ulcer history, dialysis patients, chronic renal failure patients
11.NSAID or opioid allergy
12. Pregnant and lactating women

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain score

Secondary Outcome Measures

Name	Time	Method
Postoperative patients' satisfication