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G-Tech Feasibility Study for Early Detection of a Post-op Ileus

NCT02673671 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2023-01-20

No results posted yet for this study

Summary

This feasibility study is for the purpose of determining if the G-Tech Device can differentiate between normal return of GI activity post-operatively and the myoelectric activity in patients who develop a POI.

Conditions

  • Post-operative Ileus

Interventions

DEVICE

G-Tech Myoelectric recording device

A minimum of three patches are placed on the abdomen of the patient to record myoelectric activity.

Sponsors & Collaborators

  • Eminence Clinical Research, Inc.

    collaborator INDUSTRY

  • G-Tech Corporation

    lead INDUSTRY

Principal Investigators

  • George Triadafilopoulos, MD · El Camino GI Medical Associates

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2023-12-31
Completion
2023-12-31

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 NCT02673671 on ClinicalTrials.gov