Hemoglobin Orsense and Laboratory Measurement

This study has been completed.
Sponsor:
Information provided by:
Hopital Foch
ClinicalTrials.gov Identifier:
NCT01321593
First received: March 19, 2011
Last updated: June 4, 2011
Last verified: June 2011
  Purpose

The purpose of this study is to compare the hemoglobin results obtained with the Orsense device and the Clinical Laboratory.


Condition
Emergency

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparison of the Hemoglobin Results Obtained With the Orsense Device and the Clinical Laboratory

Further study details as provided by Hopital Foch:

Primary Outcome Measures:
  • Hemoglobin measurement using the Orsense device [ Time Frame: 4 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 300
Study Start Date: February 2011
Study Completion Date: March 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts
hemogobin determination
emergency unit patients

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

emergency unit patients requiring an hemoglobin determination

Criteria

Inclusion Criteria:

  • emergency unit patients requiring an hemoglobin determination

Exclusion Criteria:

  • none
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01321593

Locations
France
Hôpital Foch
Suresnes, France, 92150
Sponsors and Collaborators
Hopital Foch
Investigators
Study Chair: Marc Fischler, MD Hôpital Foch
  More Information

No publications provided by Hopital Foch

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Pr Fischler, Hopital Foch
ClinicalTrials.gov Identifier: NCT01321593     History of Changes
Other Study ID Numbers: 2010/28
Study First Received: March 19, 2011
Last Updated: June 4, 2011
Health Authority: France: Direction Générale de la Santé

ClinicalTrials.gov processed this record on September 18, 2014