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Clinical Trials/NCT01321580
NCT01321580
Completed
Not Applicable

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

Hopital Foch1 site in 1 country300 target enrollmentStarted: January 2011Last updated:
ConditionsEmergencies

Overview

Phase
Not Applicable
Status
Completed
Enrollment
300
Locations
1
Primary Endpoint
accuracy of Masimo Pronto 7

Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • emergency unit patients requiring an hemoglobin determination

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

accuracy of Masimo Pronto 7

Time Frame: 6 months

correlation, Bland and Altman analysis

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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