Hemoglobin Measured by MASIMO SpHb™ Device and Laboratory Measurement

Comparison of the Hemoglobin Results Obtained With the Masimo SpHb™ Device and the Clinical Laboratory Measurement

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00912379

Enrollment

300

Registered

2009-06-03

Start date

2009-06-30

Completion date

2010-04-30

Last updated

2016-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients' Assessment

Brief summary

The purpose of this study is to compare the hemoglobin results obtained with the Masimo SpHb™ device and the Clinical Laboratory.

Interventions

BIOLOGICALhemoglobin determination

laboratory and non invasive hemoglobin determinations

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* emergency unit patients, PACU (post-anaesthesia care unit) and ICU patients requiring an hemoglobin determination

Exclusion criteria

* none

Design outcomes

Primary

Measure	Time frame
Accuracy of the Masimo Labs Pulse-Hemoglobin-Meter Monitor	End of the period of recruitment

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026