drugset / Trial / NCT07839715

Suzetrigine Post DIEP

NCT07839715 ↗

Phase 3 Not yet recruiting 198 enrolled Vanderbilt University Medical Center
RandomizedParallel-groupOpen-labelTreatment

Summary

This research study is being conducted to see whether adding suzetrigine (Journavx), an FDA-approved non-opioid pain medication, to the standard Enhanced Recovery After Surgery (ERAS) pain management protocol can improve pain after surgery. This is to see if we can decrease the use of opioids, since Journavx works on nerve cells outside of the brain to block pain signals and has no addictive potential. Patients will be provided suzetrigine at a pre-operative clinic visit before you come for surgery so they will have it available during your hospital stay. Oral morphine equivalents will be calculated during the inpatient and outpatient duration to assess if individuals who are assigned to the suzetrigine group have decreased use of opioids compared to the non-suzetrigine patient groups. The hypothesis is that suzetrigine will allow for decreased opioid usage.

Timeline

Start
2026-09
Primary completion
2027-08
Completion
2027-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Suzetrigine Small molecule 50 mg Oral

Indications

No indication recorded.