Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 18 and up

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

PhasePhase 4
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment150 (estimated)
SponsorHenry Ford Health System
Academic / other
Locations1 site (Grosse Pointe Farms, Michigan)
StatusRecruiting
StartedFebruary 11, 2025
Main results expectedOctober 20, 2026
Study endsOctober 20, 2026
Registry record updatedAugust 20, 2026
Trial IDNCT07775248 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

  • Henry Ford Medical Center - Grosse Pointe Cottage
    Grosse Pointe Farms, Michigan, United States
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.