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Optimal Effective Local Anesthetic Volume for Pain Relief Using Brachial Plexus Block

Post Operative Pain Clinical Trial

Official title:
Optimal Effective Local Anesthetic Volume for Pain Relief Using Brachial Plexus Block Utilizing Continuous Reassessment Method for Arthroscopic Rotator Cuff Shoulder Surgery

Clinical Trial Summary

Prospective, patient-blinded study utilizing a novel Continuous Reassessment Method that concomitantly considers both block success and block side effects (lung dysfunction) for brachial plexus nerve blocks.

Clinical Trial Description

Success or failure of the brachial plexus block for any given volume will be determined by the verbal analogue pain scale score obtained 60 minutes after surgical end time. Volumes will be determined by continuous reassessment method. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05868993
Study type Interventional
Source Benaroya Research Institute
Contact David Auyong
Phone 206-223-6980
Email anedba@vmmc.org
Status Recruiting
Phase Phase 4
Start date February 17, 2023
Completion date December 2025
View Details
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