EichorEICHOR
Study identifier: NCT05506878 Synced from ClinicalTrials.gov · August 02, 2026
● Completed

Auriculo-Nerve Stimulation on Post-Operative Opioid Requirement

Condition: Opioid Use · Auriculotherapy · Pain, Abdominal  ·  Sponsor: Jacques E. Chelly

PhaseNA
Planned participants286
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The NSS-2 BRIDGE® device (NSS stands for Neuro-Stimulation System) is a disposable device that stimulates the branches of cranial nerves and of the superficial cervical plexus innervating the ear. Because the stimulation of the nerves of the ear by the NSS-2 BRIDGE® device (NBD®) has been shown to modulate pain pathways in rodents, decrease abdominal pain in adolescents with inflammatory bile syndrome and due to the results of our preliminary pilot study, the investigators hypothesized that this technique may also be effective in reducing the requirement for postoperative opioids and provide a non-pharmacological alternative to perioperative opioid use. To establish the role that the stimulation of the nerves of the ear may have in reducing postoperative opioid requirement, the investigators are proposing to conduct a randomized, placebo controlled study in patients undergoing open abdominal or pelvic surgery requiring at least 5 days of hospitalization. Subjects who have signed an informed consent will be randomized in 2 groups (active NBD® group or inactive NBD® group). Furthermore, since preoperative and postoperative mood disorders have been shown to increase postoperative pain levels and opioid requirement by up to 50%, the investigators further hypothesize that the stimulation of the ear nerves by the NSS-2 BRIDGE® effects may be in part mediated by a reduction of the level of anxiety, depression and catastrophizing as assessed using validated questionnaires.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (4)

University of Pittsburgh Medical Center - Magee-Womens HospitalPittsburgh, Pennsylvania, United States
UPMC Montefiore HospitalPittsburgh, Pennsylvania, United States
University of Pittsburgh Medical Center - Shadyside HospitalPittsburgh, Pennsylvania, United States
University of Pittsburgh Medical Center - Passavant HospitalPittsburgh, Pennsylvania, United States

Follow this study

Save your interest here for when the public record changes — results posted, or the study's status changes. Email alerts for this study aren't switched on yet.

We keep this only about this public record, and never email you without alerts being switched on. Want it removed at any time? Email hello@eichor.com. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.

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 →