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NCT02886312 · ClinicalTrials.gov registry record

Evaluation of Oxygen Delivery Through Nasal Cannula in Volunteers

A clinical trial of Patient Comfort and Oxygen Delivery, sponsored by University of Utah.

Completed
Registry status
30
Enrollment target
1
Study location

NCT02886312 is a study of Patient Comfort and Oxygen Delivery that has completed, run by University of Utah. The registered enrollment target is 30 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT02886312, a study of Patient Comfort and Oxygen Delivery, has completed, sponsored by University of Utah.

COMPLETED
Registry status
30 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate patient comfort and oxygen delivery efficiency when providing supplemental oxygen through a nasal cannula to volunteers using an instrumented oxygen delivery system. The goals of the study are to evaluate different oxygen flow rates and oxygen delivery modes. In addition, the investigators will investigate if the system can detect apnea (cessation of breathing) and removal of the nasal cannula. The investigators will also investigate how well high flow oxygen delivered only during inspiration is tolerated and how much the end-tidal oxygen increases after two minutes of high oxygen flow delivered only during the inhalation phase of the breath.

Interventions

  • DEVICE Supplemental Oxygen Delivery System

Study Locations (1)

Utah

  • University of Utah - Salt Lake City

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2015-08
Est. Completion 2016-08

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT02886312

The ClinicalTrials.gov registry entry for NCT02886312 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Patient Comfort appearing as the primary indexed condition, and to 1 intervention - of which Supplemental Oxygen Delivery System is the first listed.

NCT02886312 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.

Frequently Asked Questions

What is clinical trial NCT02886312 about?

NCT02886312 is a clinical study titled "Evaluation of Oxygen Delivery Through Nasal Cannula in Volunteers". This study will evaluate patient comfort and oxygen delivery efficiency when providing supplemental oxygen through a nasal cannula to volunteers using an instrumented oxygen delivery system. The goals of the study are to evaluate different oxygen flow rates and oxygen delivery modes. In addition, th...

What is the current status of trial NCT02886312?

This trial is currently completed. The enrollment target is 30 participants. The study started on 2015-08. Estimated completion is 2016-08.

What conditions does trial NCT02886312 study?

This clinical trial studies the following conditions: Patient Comfort, Oxygen Delivery, Patient Monitoring.

What interventions are being tested in trial NCT02886312?

The interventions under investigation include: Supplemental Oxygen Delivery System (DEVICE).

Who is sponsoring clinical trial NCT02886312?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02886312 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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