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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07280195

ZYNRELEF vs Continuous Catheter for Pain Management Following Shoulder Arthroplasty

Status
Enrolling By Invitation
Phase
Phase 4
Study type
Interventional
Enrollment
86 (estimated)
Sponsor
Washington University School of Medicine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if local intra-operative application of ZYNRELEF (topical medication) during shoulder replacement surgery improves pain control (as defined by opioid consumption after surgery) compared to the use of an interscalene block with catheter. This is a randomized clinical trial without blinding. Subjects will complete patient reported outcomes before and after surgery. Subjects will track their narcotic use, pain scores and pain satisfaction after surgery.

Conditions

Interventions

TypeNameDescription
DRUGZynrelefZYNRELEF
DRUGBupivacaineInterscalene block with continuous catheter pump

Timeline

Start date
2026-02-14
Primary completion
2026-12-01
Completion
2027-12-01
First posted
2025-12-12
Last updated
2026-02-19

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07280195. Inclusion in this directory is not an endorsement.