Suzetrigine for Opioid-Sparing Postoperative Analgesia Following Transvaginal Pelvic Reconstructive Surgery

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of California, Los Angeles

About this trial

Suzetrigine is a selective NaV1.8 inhibitor that provides peripheral analgesia without opioid-related CNS effects. This single-center stepped-wedge randomized clinical trial evaluates whether a suzetrigine-based postoperative analgesic regimen provides non-inferior pain control compared with standard opioid-inclusive care following transvaginal pelvic reconstructive surgery. The study will enroll 120 participants and assess pain, opioid consumption, adverse events, and functional recovery.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

Undergoing elective transvaginal pelvic reconstructive surgery at UCLA with planned same-day discharge or 23-hour observation.

Able to provide written informed consent.

Disqualifiers

Chronic opioid use.

Liver failure.

End-stage renal disease (ESRD).

Contraindication to acetaminophen or ibuprofen.

Trial design

Treatments tested in this trial

  • Suzetrigine
  • Opioid Analgesics (Tramadol or Oxycodone)
  • Scheduled Acetaminophen and Ibuprofen

Treatment groups

120 Participants
are divided into 2 treatment groups