Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06648759

Vagal Stimulator to Reduce Nasogastric Tube Use

Led by Jacques E. Chelly · Updated on 2025-12-17

60

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Abdominal surgery, laparoscopic or open, is frequently performed at UPMC Shadyside hospital. One of the most frequent complications following abdominal surgery is a postoperative ileus. Although postoperative ileus may be the result of obstruction or leakage, in most cases postoperative ileus (POI) is the result of local irritation because of fluid overload, exogenous opioids, neurohormonal dysfunction, gastrointestinal stretch, local bleeding and inflammation. POI usually lasts between 2 to 7 days. In most cases, a nasogastric tube (NG tube) is used to relieve that gastric pressure until the resolution of the POI. The placement of a NG tube can lead to a local trauma, bleeding and pain. Pain represents a major complaint among those with POI, often contributing to prolonged hospital stays.

CONDITIONS

Official Title

Vagal Stimulator to Reduce Nasogastric Tube Use

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years and older undergoing laparoscopic or open colorectal surgery or other major abdominal surgeries at UPMC Shadyside
  • Development of postoperative ileus
  • Anticipation of nasogastric (NG) tube placement
Not Eligible

You will not qualify if you...

  • Pregnant individuals
  • Those unable to read, write, or speak English fluently
  • Individuals with developmental or neurological disorders unable to provide consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UPMC Shadyside Hospital

Pittsburgh, Pennsylvania, United States, 15232

Actively Recruiting

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Research Team

C

Carly Riedmann, MPH

CONTACT

A

Amy Monroe, MPH, MBA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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