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
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine 20mL 0.5% | Interscalene nerve block with 20 mL 0.5% bupivacaine. |
| DRUG | Bupivacaine 20mL 0.25% | Pecs II fascial plane block with 20 mL 0.25% bupivacaine. |
| DRUG | Bupivacaine 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04867369. Inclusion in this directory is not an endorsement.