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Predictive Validity of Acoustic Gastrointestinal Surveillance (AGIS) in Post-Operative Feeding

NCT02065583 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2015-12-11

No results posted yet for this study

Summary

This study will measure the accuracy of a disposable, non-invasive device for the continuous monitoring of abdominal sounds, called the AGIS sensor (Acoustic Gastro-Intestinal Surveillance) in predicting patients' intolerance to feeding (defined as severe nausea, vomiting, or need to place a nasogastric tube within 4 hours of initiating a standard feeding protocol) following abdominal surgery. This will be a pragmatic, observational study.

Conditions

  • Post Operative Ileus

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    collaborator OTHER

  • VA Greater Los Angeles Healthcare System

    lead FED

Principal Investigators

  • Brennan Spiegel, MD, MSHS · Cedars-Sinai Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2018-01-31
Completion
2018-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02065583 on ClinicalTrials.gov