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Detection of Silent Aspiration Events Utilizing pH/Impedance Probes in Hospitalized Patients

NCT02720029 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-01-25

No results posted yet for this study

Summary

Monitoring and quantification of reflux events in high risk critically ill inpatients and lower risk general medical/surgical inpatients, with comparison to relevant clinical variables.

Conditions

  • Acid Aspiration Syndrome

Interventions

DEVICE

pH/impedance monitor

Placement of pH/impedance monitor via the nasogastric route with monitoring for 24 hours, followed by removal.

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • Joshua P Fessel, MD, PhD · Vanderbilt University

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2019-04-30
Completion
2019-04-30

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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 NCT02720029 on ClinicalTrials.gov