Clinical Trials Directory

Trials / Completed

CompletedNCT04867369

Pecs II Block Versus Surgeon Infiltration for Open Subpectoral Biceps Tenodesis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
160 (actual)
Sponsor
NYU Langone Health · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGBupivacaine 20mL 0.5%Interscalene nerve block with 20 mL 0.5% bupivacaine.
DRUGBupivacaine 20mL 0.25%Pecs II fascial plane block with 20 mL 0.25% bupivacaine.
DRUGBupivacaine up to 15mL 0.25%Local infiltration of 0.25% bupivacaine by the surgeon, up to 15 mL.

Timeline

Start date
2021-07-14
Primary completion
2023-11-08
Completion
2023-11-11
First posted
2021-04-30
Last updated
2024-12-13
Results posted
2024-12-13

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04867369. Inclusion in this directory is not an endorsement.

Pecs II Block Versus Surgeon Infiltration for Open Subpectoral Biceps Tenodesis (NCT04867369) · Clinical Trials Directory