Hemoglobin MASIMO (Pronto 7) and Laboratory Measurement

Hopital Foch

Status: Completed

Conditions: Emergencies

Treatments: Device: Masimo Pronto 7

Study type: Interventional

Funder types: Other

Identifiers

NCT01321580

2010/43

2010-A00541-38 (Other Identifier)

Details and patient eligibility

About

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

Enrollment: 300 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• emergency unit patients requiring an hemoglobin determination

Exclusion criteria

• none

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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300 participants in 1 patient group

Group A

Experimental group

Treatment:

Device: Masimo Pronto 7