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Suzetrigine in TKA

NCT07864896

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

Total knee replacements are among the most common and painful orthopedic procedures performed worldwide, often requiring intensive analgesia to support early ambulation and recovery. Despite widespread use of multimodal regimens, many patients still rely on opioids, which can cause sedation, nausea, constipation, and long-term dependency. Evaluating suzetrigine in this high-need population may improve recovery trajectories, reduce opioid consumption, and support enhanced recovery protocols.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Total Knee Arthroplasty (TKA)
  • Total Knee Arthroplasty \(TKA\)
  • Total Knee Replacement
  • Total Knee Replacement Surgery
  • Total Knee Replacements
  • Total Knee Replacement Arthroplasty
  • Suzetrigine
  • Pain Management
  • Pain
  • Nav 1.8
  • JOURNAVX
  • Opioid Cessation
  • Opioid Consumption, Postoperative
  • Multimodal Analgesia
  • Randomized Controlled Trial
  • Randomized Controlled Study
  • Randomized Controlled Trials

Eligibility basics and study details

Study type
Interventional
Phase
Phase 3
Ages
18 to 80 years
Sex
All
Healthy volunteers
Accepted
Sponsor
Hospital for Special Surgery, New York
Last updated on ClinicalTrials.gov
October 13, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

New York · 1

  • Hospital for Special Surgery · New York, NY

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.