Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05506878

Auriculo-Nerve Stimulation on Post-Operative Opioid Requirement

Led by Jacques E. Chelly · Updated on 2026-01-08

286

Participants Needed

4

Research Sites

205 weeks

Total Duration

On this page

Sponsors

J

Jacques E. Chelly

Lead Sponsor

M

Masimo Corporation

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Auriculo-Nerve Stimulation on Post-Operative Opioid Requirement

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 years of age
  • Scheduled for elective open primary abdominal and pelvic colorectal cancer resection surgery or living-donor liver transplant surgery following the ERAS protocol
  • Expected hospital stay of approximately 5 days
Not Eligible

You will not qualify if you...

  • Unable to give consent as determined by medical or surgical team
  • Clinical evidence of anxiety, depression, or suicidal ideation based on medical history and psychosocial testing
  • Chronic pain conditions or daily opioid use of 60 mg oral morphine equivalent or more
  • True allergy to all opioid medications
  • History or current alcohol or drug abuse for at least 3 months
  • Surgery performed laparoscopically
  • Non-elective surgery
  • Pregnancy
  • Contraindications to NSS-2 BRIDGE use, including cardiac pacemaker, hemophilia, psoriasis, or ear eczema
  • Post-surgery intubation with sedation or fentanyl infusion
  • Rapid recovery surgeries
  • Diagnosed seizure disorder
  • Use of dexmedetomidine in ICU

AI-Screening

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Trial Site Locations

Total: 4 locations

1

University of Pittsburgh Medical Center - Magee-Womens Hospital

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

2

UPMC Montefiore Hospital

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

3

University of Pittsburgh Medical Center - Shadyside Hospital

Pittsburgh, Pennsylvania, United States, 15232

Actively Recruiting

4

University of Pittsburgh Medical Center - Passavant Hospital

Pittsburgh, Pennsylvania, United States, 15237

Actively Recruiting

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Research Team

A

Amy Monroe, MPH, MBA

CONTACT

C

Carly Riedmann, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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