Hemoglobin Measured by "Orsense NBM-200MP" Device and Laboratory Measurement
Comparison of the Hemoglobin Results Obtained With the "Orsense NBM-200MP" Device and the Clinical Laboratory
2 other identifiers
observational
300
1 country
1
Brief Summary
The purpose of this study is to compare the hemoglobin results obtained with the "Orsense NBM-200MP" device and the Clinical Laboratory.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2011
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
March 19, 2011
CompletedFirst Posted
Study publicly available on registry
March 23, 2011
CompletedNovember 3, 2016
November 1, 2016
28 days
March 19, 2011
November 2, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
Hemoglobin measurement using the "Orsense NBM-200MP" device
4 months
Study Arms (1)
hemoglobin determination
emergency unit patients
Eligibility Criteria
emergency unit patients requiring an hemoglobin determination
You may qualify if:
- emergency unit patients requiring an hemoglobin determination
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Hopital Fochlead
Study Sites (1)
Hôpital Foch
Suresnes, 92150, France
Related Publications (1)
Gayat E, Aulagnier J, Matthieu E, Boisson M, Fischler M. Non-invasive measurement of hemoglobin: assessment of two different point-of-care technologies. PLoS One. 2012;7(1):e30065. doi: 10.1371/journal.pone.0030065. Epub 2012 Jan 6.
PMID: 22238693DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Marc Fischler, MD
Hôpital Foch
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 19, 2011
First Posted
March 23, 2011
Study Start
February 1, 2011
Primary Completion
March 1, 2011
Study Completion
March 1, 2011
Last Updated
November 3, 2016
Record last verified: 2016-11