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Clinical Trial Summary

A phase IV, randomized, single-blind, single-center study measuring the effects of Pecs II block with 0.25% bupivacaine versus surgeon infiltration with 0.25% bupivacaine on postoperative pain control and opioid utilization in participants who undergo open subpectoral tenodesis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04867369
Study type Interventional
Source NYU Langone Health
Contact Uchenna Umeh, MD
Phone 212-598-6085
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date May 3, 2021
Completion date August 7, 2023

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