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Hemoglobin MASIMO (Pronto 7) and Laboratory Measurement

Comparison of the Hemoglobin Results Obtained With the Masimo Pronto 7 and the Clinical Laboratory Measurement Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01321580
Enrollment
300
Registered
2011-03-23
Start date
2011-01-31
Completion date
2011-02-28
Last updated
2016-11-03

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

Conditions

Emergencies

Brief summary

The purpose of this study is to compare the hemoglobin results obtained with the Masimo Pronto 7 and the Clinical Laboratory.

Interventions

DEVICEMasimo Pronto 7

non invasive hemoglobin determination by the Masimo Pronto 7 versus laboratory hemoglobin measurement

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* emergency unit patients requiring an hemoglobin determination

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
accuracy of Masimo Pronto 76 monthscorrelation, Bland and Altman analysis

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026