Actively Recruiting
Comparison of Postoperative Quality of Recovery by Anesthetic Method in Patients Undergoing Shoulder Arthroscopy
Led by Seoul National University Hospital · Updated on 2025-05-15
140
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to compare the quality of recovery in patients undergoing arthroscopic shoulder surgery depending on the type of anesthesia used: 1. general anesthesia with preoperative brachial plexus block for intra- and postoperative analgesia 2. regional anesthesia (brachial plexus block) with intraoperative sedation.
CONDITIONS
Official Title
Comparison of Postoperative Quality of Recovery by Anesthetic Method in Patients Undergoing Shoulder Arthroscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients of age 19 years and above, scheduled for shoulder arthroscopic surgery
You will not qualify if you...
- Emergency operation
- Inflammation or infection at the site of nerve block administration
- Inability to perform the quality of recovery questionnaire due to dementia or delirium
- Severe lung disease (e.g. chronic obstructive pulmonary disease or interstitial lung disease)
- Contraindication to brachial plexus block
- History of hypersensitivity or side effect to ropivacaine
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Seoul National University Hospital
Seoul, Jongno-gu, South Korea, 03080
Actively Recruiting
Research Team
H
Hansol Kim, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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