Hemoglobin Measured by MASIMO SpHb™ Device and Laboratory Measurement

Completed

• Conditions: Patients' Assessment
• Interventions: Biological: hemoglobin determination

• Registration Number: NCT00912379
• Lead Sponsor: Hopital Foch

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2009-06
• Study First Submitted: 2009-06-01
• Study First Submitted QC: 2009-06-02
• Study First Posted: 2009-06-03
• Primary Completion: 2010-04
• Study Completion: 2010-04
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-23
• Last Update Posted: 2016-09-26

Recruitment & Eligibility

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

Inclusion Criteria

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

Read More

Exclusion Criteria

• none

Read More

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
hemoglobin determination	hemoglobin determination	ICU and emergency unit patients

Primary Outcome Measures

Name	Time	Method
Accuracy of the Masimo Labs Pulse-Hemoglobin-Meter Monitor	End of the period of recruitment

Trial Locations

Locations (1)

Hôpital Foch; 🇫🇷 Suresnes, France