Hemoglobin MASIMO (Pronto 7) and Laboratory Measurement

Not Applicable

Completed

• Conditions: Emergencies
• Interventions: Device: Masimo Pronto 7

• Registration Number: NCT01321580
• Lead Sponsor: Hopital Foch

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2011-01
• Primary Completion: 2011-02
• Study Completion: 2011-02
• Study First Submitted: 2011-03-19
• Study First Submitted QC: 2011-03-22
• Study First Posted: 2011-03-23
• Status Verified: 2016-11
• Last Update Submitted: 2016-11-02
• Last Update Posted: 2016-11-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• emergency unit patients requiring an hemoglobin determination

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Exclusion Criteria

• none

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Group A	Masimo Pronto 7	-

Primary Outcome Measures

Name	Time	Method
accuracy of Masimo Pronto 7	6 months	correlation, Bland and Altman analysis

Trial Locations

Locations (1)

Hôpital Foch; 🇫🇷 Suresnes, France