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Clinical Trials/NCT03125018
NCT03125018CompletedNot Applicable

Accuracy of SpO2 for Noninvasive Pulse Oximeter Sensor (LNCS ADTX)

Masimo Corporation2 sites in 1 country13 target enrollmentStarted: September 30, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
13
Locations
2
Primary Endpoint
Accuracy of Sensor by Arms Calculation

Study Overview

Brief Summary

In this study, the level of oxygen within the blood will be reduced in a controlled manner by reducing the concentration of oxygen the study volunteer breathes. The accuracy of a noninvasive pulse oximeter sensor will be assessed by comparison to the oxygen saturation measurements from a laboratory blood gas analyzer.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Competent non-smoking adults between the ages of 18 and 40 for each series of tests.
  • Subjects must understand and consent to be in the study.
  • American Society of Anesthesiology Class 1 (Healthy subjects without any systemic disease at all).

Exclusion Criteria

  • Subjects who have any systemic disease at all.
  • Subjects who do not understand the study and the risks.
  • Subjects who are pregnant.
  • Subjects having either signs or history of peripheral ischemia.
  • Others deemed ineligible by the clinical staff.

Arms & Interventions

Test Subject

Experimental

All subjects are enrolled into the test group and receive the LNCS ADTX Sensor.

Intervention: LNCS ADTX Sensor (Device)

Outcomes

Primary Outcomes

Accuracy of Sensor by Arms Calculation

Time Frame: 1-5 hours

Accuracy will be determined by comparing the noninvasive blood oxygen saturation measurement of the pulse oximeter to that obtained from a blood sample and calculating the arithmetic root mean square error (Arms) value. In order to obtain the Arms value, the blood oxygen saturation measurement is subtracted from the pulse oximeter oxygen saturation measurement for a number of samples, the average of this difference is computed as the bias. The standard deviation of the differences is computed as the precision. The square root of the sum of the squares of bias and precision is computed as the Arms Error value.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (2)

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