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Hemoglobin MASIMO (Pronto 7) and Laboratory Measurement

Not Applicable
Completed
Conditions
Emergencies
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

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • emergency unit patients requiring an hemoglobin determination
Exclusion Criteria
  • none

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
accuracy of Masimo Pronto 76 months

correlation, Bland and Altman analysis

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hôpital Foch

🇫🇷

Suresnes, France

Hôpital Foch
🇫🇷Suresnes, France

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