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NOT YET RECRUITING
NCT07839715
PHASE3

Suzetrigine Post DIEP

Sponsor: Vanderbilt University Medical Center

View on ClinicalTrials.gov

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.

Official title: Evaluation of Suzetrigine Within an ERAS Protocol for DIEP Flap Breast Reconstruction: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

198

Start Date

2026-09

Completion Date

2027-08

Last Updated

2026-09-24

Healthy Volunteers

No

Interventions

DRUG

Suzetrigine Group

Patients after DIEP getting both ERAS protocol with suzetrigine