Completed

NCT Number: NCT00912379

Hemoglobin Measured by MASIMO SpHb™ Device and Laboratory Measurement

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

Completed

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Key information

Conditions

Patients' Assessment

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpital Foch

Suresnes, 92151, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

emergency unit patients, PACU (post-anaesthesia care unit) and ICU patients requiring an hemoglobin determination

Exclusion criteria

none

Treatment and study plan

hemoglobin determination

Biological

laboratory and non invasive hemoglobin determinations

Primary outcomes

Accuracy of the Masimo Labs Pulse-Hemoglobin-Meter Monitor

Time frame: End of the period of recruitment

Sponsors and collaborators

Lead sponsor

Hopital Foch

Other

Registry information

Official study title

Comparison of the Hemoglobin Results Obtained With the Masimo SpHb™ Device and the Clinical Laboratory Measurement

Important dates

Study start: 2009
Primary completion: 2010
Study completion: 2010
First posted: Jun 3, 2009
Registry last updated: Sep 26, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.