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NCT01321593 Clinical Trial

Hemoglobin Measured by "Orsense NBM-200MP" Device and Laboratory Measurement

Emergency Clinical Trial

Official title:
Comparison of the Hemoglobin Results Obtained With the "Orsense NBM-200MP" Device and the Clinical Laboratory

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01321593
Other study ID # 2010/28
Secondary ID 2010-A00541-38
Status Completed
Phase N/A
First received March 19, 2011
Last updated November 2, 2016
Start date February 2011
Est. completion date March 2011

Study information
Verified date November 2016
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority France: Direction Générale de la Santé
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare the hemoglobin results obtained with the "Orsense NBM-200MP" device and the Clinical Laboratory.

Recruitment information / eligibility
Status Completed
Enrollment 300
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- emergency unit patients requiring an hemoglobin determination

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France Hôpital Foch Suresnes

Sponsors (1)
Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hemoglobin measurement using the "Orsense NBM-200MP" device 4 months No
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