← Eichor
Study identifier: NCT07633444 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Transauricular Vagus Nerve Stimulation Frequencies for Postoperative Pain

Condition: Postoperative Pain · Postoperative Nausea and Vomiting (PONV) · Opioid Consumption, Postoperative  ·  Sponsor: Federal University of Bahia

PhaseNA
Planned participants174
Who can joinAll sexes, 18 Years to 59 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn whether different frequencies of transauricular vagus nerve stimulation (tVNS) can reduce postoperative pain and opioid consumption in adults undergoing abdominal or urologic surgery. It will also evaluate the effects of tVNS on recovery quality, autonomic function, and treatment safety. The main questions it aims to answer are: Does transauricular vagus nerve stimulation reduce postoperative opioid consumption during the first 24 hours after surgery? Do different stimulation frequencies (high-frequency and low-frequency tVNS) produce different effects on postoperative pain and autonomic responses? Is transauricular vagus nerve stimulation safe and well tolerated in surgical patients? Researchers will compare high-frequency tVNS, low-frequency tVNS, and sham stimulation (inactive stimulation) to determine their effects on postoperative pain and opioid requirements. Participants will: Be randomly assigned to receive high-frequency tVNS, low-frequency tVNS, or sham stimulation. Receive two 30-minute stimulation sessions, one before anesthesia and one after surgery in the post-anesthesia care unit. Undergo assessments of postoperative pain, opioid consumption, need for rescue analgesics, postoperative nausea and vomiting, heart rate changes, and quality of recovery. Be monitored for adverse events related to the intervention during the study period. A total of 174 participants will be enrolled in this single-center, randomized,…

This description comes directly from the study's public registry record.

Talk to the study team

Rodrigo L Alves, MD, PhD  ·  71 99961-9818  ·  rlalves@ufba.br

João Paulo A de Carvalho  ·  75 98295-3834  ·  joaoaureliano@ufba.br

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Universitário Professor Edgard Santos, Federal University of Bahia (HUPES-UFBA)Salvador, Estado de Bahia, BrazilRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07633444