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Comparison of Using CIBPB With or Without IV-PCA After Arthroscopic Rotator Cuff Repair

Brachial Plexus Block Clinical Trial

Official title:
Comparison of Quality of Recovery in Patients Using Continuous Brachial Plexus Block With or Without Intravenous Patient-Controlled Analgesia After Arthroscopic Rotator Cuff Repair: A Prospective Randomized Study

Clinical Trial Summary

The goal of this study is to compare the continuous brachial plexus block with or without intravenous patient controlled analgesia(PCA) in patients undergoing arthroscopic rotator cuff repair, in terms of quality of recovery, postoperative pain score, and adverse event.

Clinical Trial Description

The Bellomic® M silicone balloon infuser, dual continuous petite type (cebika, Uiwang-si, Gyeonggi-do, Republic of Korea) has 2-channel infusion elastomeric pump with two balloon chambers. This structure allows the simultaneous use of continuous nerve block and intravenous PCA. In addition, intravenous PCA can be continued even when continuous nerve block is discontinued due to discomfort such as numbness, tingling sense or motor block. This is expected to contribute to the patient satisfaction and quality of recovery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05691101
Study type Interventional
Source Seoul National University Bundang Hospital
Contact JI IN PARK
Phone 82 10 3077 3666
Email monica0120120@gmail.com
Status Recruiting
Phase N/A
Start date January 31, 2023
Completion date December 31, 2023
View Details
See also
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