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Accuracy of Noninvasive Rainbow Adhesive R1 Pulse Oximeter Sensor

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Masimo

Status

Completed

Conditions

Healthy

Treatments

Device: Rainbow Adhesive Noninvasive R1 Pulse Oximeter Sensor

Study type

Interventional

Funder types

Industry

Identifiers

NCT03134313
TR18670-1029

Details and patient eligibility

About

In this study, the concentration of hemoglobin will be measured using a noninvasive pulse oximeter sensor and compared with the hemoglobin value from a blood sample of the volunteer. The accuracy of a noninvasive hemoglobin sensor(s) will be assessed by comparison to hemoglobin measurements from a laboratory analyzer.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Greater than 18 years old
  • Healthy

Exclusion criteria

  • Do not understand the study and the risks involved
  • Deemed ineligible by study test personnel

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

R1-25 Sensor
Experimental group
Description:
All subjects will be enrolled in the test group and will receive Rainbow Adhesive Noninvasive R1 Pulse Oximeter Sensor
Treatment:
Device: Rainbow Adhesive Noninvasive R1 Pulse Oximeter Sensor

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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