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CompletedNCT00912379Updated Sep 26, 2016

Hemoglobin Measured by MASIMO SpHb™ Device and Laboratory Measurement

An observational study in Patients' Assessment, sponsored by Hopital Foch. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-09-26.

Sponsored by Hopital Foch · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

  • Patients' Assessment
03

In context

Lead sponsor

Hopital Foch is the lead sponsor of 208 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

emergency unit patients and ICU patients requiring an hemoglobin determination

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (actual)

Groups and cohorts

  • hemoglobin determination

    ICU and emergency unit patients

    Biological: hemoglobin determination

Interventions

  • Biologicalhemoglobin determination

    laboratory and non invasive hemoglobin determinations

06

What researchers measure

Primary outcomes

  1. Accuracy of the Masimo Labs Pulse-Hemoglobin-Meter Monitor

    Time frame: End of the period of recruitment

07

Study locations

1 site
  • Hôpital Foch
    Suresnes, 92151, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 26, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00912379
Lead sponsor
Hopital Foch
Responsible party
Sponsor
First posted
Jun 3, 2009
Start date
Jun 2009
Primary completion
Apr 2010
Completion
Apr 2010
Last update
Sep 26, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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