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NCT02892513 · ClinicalTrials.gov registry record · NA

Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults

A NA study, sponsored by Medical College of Wisconsin.

Completed
Registry status
NA
Development phase
53
Enrollment target

NCT02892513: Completed NA study, sponsored by Medical College of Wisconsin.

NCT02892513 is a NA study that has completed, run by Medical College of Wisconsin. The registered enrollment target is 53 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02892513, a NA study, has completed, sponsored by Medical College of Wisconsin.

COMPLETED
Registry status
NA
Development phase
53 participants
Enrollment target

Study Summary

Pain after surgery is unavoidable, and opioid medications are the cornerstone of most pain management regimens. However, they come at a cost with profound impacts on gastrointestinal motility, respiratory depression, and even long-term dependence. Stimulating the external ear with cutaneous electrical current is similar to acupuncture and could help improve postoperative pain. The Bridge device (manufactured by Key Electronics \[Jeffersonville, IN, USA\] and distributed by Innovative Health Solutions \[Versailles, IN, USA\]), has been used with success in treating opioid withdrawal and in animal studies has shown increases in pain thresholds. The investigators propose a prospective, randomized, placebo-controlled, double-blinded trial to evaluate if auricular neurostimulation improves postoperative pain and reduces opioid requirements for patients undergoing elective colon surgery. pain perception in post-operative patients may be modulated via the auricular branch of the vagus nerve. This has the potential to reduce the use of opioid medications, which will in turn reduce the incidence of postoperative ileus and reduce patient need for and dependence on narcotic pain medications. This would have an enormous economic impact due to decreased length of hospital stays for patients who undergo abdominal surgery. In addition, opioid reduction could potentially lessen the national crisis of opioid addiction.

Primary Outcome

Total inpatient narcotic use measured in oral morphine equivalents per day (OME)

Interventions

  • DEVICE Percutaneous auricular neurostimulation
  • DEVICE Sham percutaneous auricular neurostimulation

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2016-11
Est. Completion 2018-04-30
Phase NA
Medical College of Wisconsin

447 total trials

What the finished NCT02892513 record still lists

NCT02892513 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Percutaneous auricular neurostimulation is the first listed.

NCT02892513 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02892513 about?

NCT02892513 is a clinical study titled "Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults". Pain after surgery is unavoidable, and opioid medications are the cornerstone of most pain management regimens. However, they come at a cost with profound impacts on gastrointestinal motility, respiratory depression, and even long-term dependence. Stimulating the external ear with cutaneous electric...

What is the current status of trial NCT02892513?

This trial is currently completed. It is a NA study. The enrollment target is 53 participants. The study started on 2016-11. Estimated completion is 2018-04-30.

What interventions are being tested in trial NCT02892513?

The interventions under investigation include: Percutaneous auricular neurostimulation (DEVICE), Sham percutaneous auricular neurostimulation (DEVICE).

Who is sponsoring clinical trial NCT02892513?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02892513's enrollment target sits among peer trials

53 1271st of 2000 higher than 729 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02892513, the US trial registry maintained by the National Library of Medicine. NCT02892513 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.