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NCT03279458 · ClinicalTrials.gov registry record · NA

Non-invasive Tidal Volume Monitoring Using the Linshom Respiratory Monitoring Device

A NA study, sponsored by University of Mississippi Medical Center.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT03279458 is a NA study that has completed, run by University of Mississippi Medical Center. The registered enrollment target is 40 participants.

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The verdict

NCT03279458, a NA study, has completed, sponsored by University of Mississippi Medical Center.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

Many post-operative complications arise from patients who breathe inadequately. Inadequate respiration, whether the result of surgery or the anesthesia, causes a decrease in blood oxygen saturation and an increase in carbon dioxide partial pressure. Both of these surrogate measurements of respiration may pose a challenge to measure. Some administer exogenous oxygen to all patients as they leave the operating room in order to maintain the blood oxygen saturation. This renders the oximeter a less sensitive metric of depressed respiration. In the face of decreased respiration, the carbon dioxide levels continue to increase slowly and often go undetected unless blood gases are measured. Indeed carbon dioxide blood levels are the only metric to detect inadequate ventilation using this surrogate index. Monitoring ventilation is a serious challenge outside of critical care settings. In fact, there are no monitors available that can measure tidal volume or relative tidal volume outside of these settings. Linshom is a novel instrument that tracks relative respiration by measuring the excursions of the temperature swings between inspiration and expiration and normalizing them to the patient's breathing. This monitor may be the first non-invasive monitor to measure relative tidal volume in non-critical care settings. The purpose of this study is to determine whether a non-invasive, temperature-based respiratory instrument can track tidal volume (Vt) in patients. The investigators hypothesize that the Linshom device can accurately and consistently track tidal volume as measured by closed loop mechanical ventilator.

Interventions

  • DEVICE Linshom Respiratory Monitoring Device

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2017-09-08
Est. Completion 2017-09-08
Phase NA

What the Registry Record Tells You About NCT03279458

The ClinicalTrials.gov registry entry for NCT03279458 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Mississippi Medical Center, which has 96 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Linshom Respiratory Monitoring Device is the first listed.

NCT03279458 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03279458 about?

NCT03279458 is a clinical study titled "Non-invasive Tidal Volume Monitoring Using the Linshom Respiratory Monitoring Device". Many post-operative complications arise from patients who breathe inadequately. Inadequate respiration, whether the result of surgery or the anesthesia, causes a decrease in blood oxygen saturation and an increase in carbon dioxide partial pressure. Both of these surrogate measurements of respiratio...

What is the current status of trial NCT03279458?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2017-09-08. Estimated completion is 2017-09-08.

What interventions are being tested in trial NCT03279458?

The interventions under investigation include: Linshom Respiratory Monitoring Device (DEVICE).

Who is sponsoring clinical trial NCT03279458?

This trial is sponsored by University of Mississippi Medical Center, which has 96 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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