Masimo CO-Oximeter Study

This is a study to evaluate the accuracy of the Masimo Rainbow SET Pulse CO-Oximeter in monitoring the hemoglobin levels of patients undergoing isovolemic hemodilution.

Completed

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Key information

Conditions

Cardiac Surgical Procedures

Sex eligibility

All sexes

Study type

Observational

Primary location

Nationwide Children's Hospital

Columbus, Ohio, 43147, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Any subject that is scheduled to have isovolemic hemodilution

Exclusion criteria

Anything that prevents a subject from having isovolemic hemodilution

Treatment and study plan

Primary outcomes

hemoglobin value

Time frame: 1 Day (day of surgery)

The accuracy of the hemoglobin value from the Masimo pulse oximeter during isovolemic hemodilution.

Sponsors and collaborators

Lead sponsor

Nationwide Children's Hospital

Other

Registry information

Official study title

Use of the Masimo Rainbow SET Pulse CO-Oximeter in Patients Undergoing Isovolemic Hemodilution

Important dates

Study start: 2010
Primary completion: 2011
Study completion: 2011
First posted: Aug 19, 2010
Registry last updated: Jan 31, 2012

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.

Published trials that share one or more normalized conditions with this study.

Completed