Emergency
Conditions
Brief summary
The purpose of this study is to compare the hemoglobin results obtained with the Orsense NBM-200MP device and the Clinical Laboratory.
Interventions
None listed
Sponsors
Hopital Foch
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* emergency unit patients requiring an hemoglobin determination
Exclusion criteria
* none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hemoglobin measurement using the Orsense NBM-200MP device | 4 months |
Countries
France
Outcome results
None listed