Viewing Study NCT05868993


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Ignite Modification Date: 2025-12-25 @ 11:17 PM
Study NCT ID: NCT05868993
Status: RECRUITING
Last Update Posted: 2023-05-22
First Post: 2023-04-27
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Optimal Effective Local Anesthetic Volume for Pain Relief Using Brachial Plexus Block
Sponsor: Benaroya Research Institute
Organization:

Study Overview

Official Title: Optimal Effective Local Anesthetic Volume for Pain Relief Using Brachial Plexus Block Utilizing Continuous Reassessment Method for Arthroscopic Rotator Cuff Shoulder Surgery
Status: RECRUITING
Status Verified Date: 2023-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed 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 Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: