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NCT05691101
Comparison of Using CIBPB With or Without IV-PCA After Arthroscopic Rotator Cuff Repair
Conditions: Analgesia, Patient-Controlled, Brachial Plexus Block, Arthroscopic Rotator Cuff Repair
Sex: All
Ages: 20 Years – 69 Years
Phase: NA
Enrollment: 80
Sponsor: Seoul National University Bundang Hospital
Location: Korea, Republic of
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.
Eligibility Criteria
Inclusion Criteria:Having arthroscopic rotator cuff repairAmerican Society of Anesthesiologists physical status I-IIIExclusion Criteria:Contraindication to interscalene brachial plexus blockContraindication to fentanyl
Source: ClinicalTrials.gov (NCT05691101). StuddyBuddy aggregates publicly available trial information.
