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
| Type | Name | Description |
|---|---|---|
| DRUG | Zynrelef | ZYNRELEF |
| DRUG | Bupivacaine | Interscalene 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07280195. Inclusion in this directory is not an endorsement.