NCT01321593
Completed
Not Applicable
Comparison of the Hemoglobin Results Obtained With the "Orsense NBM-200MP" Device and the Clinical Laboratory
ConditionsEmergency
Overview
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Hopital Foch
- Enrollment
- 300
- Locations
- 1
- Primary Endpoint
- Hemoglobin measurement using the "Orsense NBM-200MP" device
Overview
Brief Summary
The purpose of this study is to compare the hemoglobin results obtained with the "Orsense NBM-200MP" device and the Clinical Laboratory.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
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
Hemoglobin measurement using the "Orsense NBM-200MP" device
Time Frame: 4 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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