A Retrospective Observational Study of Operating Room Efficiency Operation with Pre-insertion of Brachial Plexus Block Catheter in Shoulder Arthroplasty
Not Applicable
- Conditions
- rotator cuff tear
- Registration Number
- JPRN-UMIN000050260
- Lead Sponsor
- Gunma University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 148
Inclusion Criteria
Not provided
Exclusion Criteria
An open letter will be prepared and patients will be excluded from the study if they are informed that they do not wish to be included in the study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is to compare the time from patient admission to the start of general anesthesia between the catheter pre-insertion group and the catheter pre-insertion group as a control group to determine whether catheter pre-insertion contributes to operating room efficiency.
- Secondary Outcome Measures
Name Time Method As a secondary outcome, we would like to examine whether catheter preinsertion is disadvantageous to patients by comparing the use of remifentanil, an analgesic used during surgery, the postoperative resting shoulder pain numerical rating scale (NRS), and the rate of catheter reinsertion. The results of this study will be presented at the end of the study. In addition, we would like to compare the time of leaving the operating room before and after pre-catheter insertion in shoulder joint surgery patients, and to examine whether the overtime hours of medical staff could be reduced.