Accuracy of Noninvasive Pulse Oximeter Sensor (LNCS DBI)
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|ClinicalTrials.gov Identifier: NCT03124979|
Recruitment Status : Completed
First Posted : April 24, 2017
Results First Posted : July 28, 2017
Last Update Posted : July 28, 2017
|Condition or disease||Intervention/treatment||Phase|
|Healthy||Device: LNCS DBI Sensor||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||13 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Actual Study Start Date :||January 18, 2012|
|Actual Primary Completion Date :||April 10, 2012|
|Actual Study Completion Date :||April 10, 2012|
All subjects are enrolled into the test group and all subjects received the LNCS DBI Sensor.
Device: LNCS DBI Sensor
Noninvasive Measurement of SpO2
- 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(Arms) error 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 these 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03124979
|United States, California|
|Irvine, California, United States, 92618|