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NCT02382133 · ClinicalTrials.gov registry record · NA

Comparison of Nasal and Forehead Oximetry in Critically Ill Patients at Risk for Decreased Peripheral Perfusion

A NA study, sponsored by Washington University School of Medicine.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT02382133 is a NA study that has completed, run by Washington University School of Medicine. The registered enrollment target is 43 participants.

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The verdict

NCT02382133, a NA study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

Continuous pulse oximetry monitoring is the standard of care in critically ill patients in emergency departments, operating rooms and intensive care units. In patients with poor peripheral perfusion (low blood flow) due to peripheral vascular disease, low body temperature, or shock and the use of medications to raise the blood pressure, clinicians have difficulty obtaining an accurate measurement. This study compares the accuracy of forehead oximetry sensors to nasal alar sensors to lab oximetry measures and on the rate of device related pressure ulcers with both.

Interventions

  • DEVICE Nasal alar oxygen sensor

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2014-10
Est. Completion 2016-09
Phase NA

What the Registry Record Tells You About NCT02382133

The ClinicalTrials.gov registry entry for NCT02382133 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Nasal alar oxygen sensor is the first listed.

NCT02382133 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02382133 about?

NCT02382133 is a clinical study titled "Comparison of Nasal and Forehead Oximetry in Critically Ill Patients at Risk for Decreased Peripheral Perfusion". Continuous pulse oximetry monitoring is the standard of care in critically ill patients in emergency departments, operating rooms and intensive care units. In patients with poor peripheral perfusion (low blood flow) due to peripheral vascular disease, low body temperature, or shock and the use of me...

What is the current status of trial NCT02382133?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2014-10. Estimated completion is 2016-09.

What interventions are being tested in trial NCT02382133?

The interventions under investigation include: Nasal alar oxygen sensor (DEVICE).

Who is sponsoring clinical trial NCT02382133?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.