Long-acting local pain medicine after knee replacement
Official title: Novel Extended-Release Bupivacaine Polymer for Sustained Pain Relief Following Total Knee Arthroplasty
Run by Henry Ford Health System · NCT07775248 · Data updated 2026-11-12
This study tests whether a new extended-release pain medicine (Zynrelef) given around the knee during total knee replacement can reduce pain after surgery better or as well as standard injections or nerve blocks.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Henry Ford Health System Academic / other |
| Locations | 1 site (Grosse Pointe Farms, Michigan) |
| Status | Recruiting |
| Started | February 11, 2025 |
| Main results expected | October 20, 2026 |
| Study ends | October 20, 2026 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT07775248 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older having primary total knee replacement by fellowship-trained orthopedic surgeons at Henry Ford Health System.
✕Probably not a fit
Patients who do not experience improved pain control or who have contraindications to the study medications may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults undergoing first-time knee replacement are randomized to receive one of three pain-control approaches during surgery: a standard knee injection, an adductor canal nerve block, or a periarticular injection containing bupivacaine and meloxicam. The goal is to see if the long-acting Zynrelef formulation provides sustained pain relief with fewer opioid needs compared with the other methods. The trial is conducted in a real-world setting within the Henry Ford Health System, with same-day discharge as a likelihood. Outcomes focus on pain control in the immediate postoperative period and opioid consumption, among other safety measures. This Phase 4 study aims to determine whether this new treatment can improve recovery after knee arthroplasty compared with current practices.
Why it matters
Potential benefit: If successful, patients could experience better pain control after knee replacement and reduced need for opioids.
How similar studies have gone: Previous similar approaches have shown potential for extended-release local anesthetics to improve postoperative pain, but results vary by method and setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients age 18 and older undergoing primary total knee replacement by fellowship trained Orthopedic Surgeons in Henry Ford Health System with planned outpatient same-day discharge. Exclusion Criteria: * Incomplete data in medical records * Non-English speakers * Chronic opioid use in the last 3 months * Ipsilateral joint surgery in the last year * Undergoing bilateral knee arthroplasty * Cannot tolerate oral medications * Swallowing difficulties * Intolerance to acetaminophen, anti-inflammatories, muscle relaxants, gabapentinoids, or opioids/tramadol * History of alcohol abuse * Drug abuse * Renal impairment * Peptic ulcer disease * GI bleeding * Illicit narcotic usage in the past 6 months * Chronic liver disease * Chronic pain syndromes
Where it's running
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Henry Ford Medical Center - Grosse Pointe Cottage
Grosse Pointe Farms, Michigan, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.