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Clinical Trials/NCT01184521
NCT01184521CompletedNot Applicable

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

Nationwide Children's Hospital1 site in 1 country50 target enrollmentStarted: September 2010Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
hemoglobin value
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Any subject that is scheduled to have isovolemic hemodilution

Exclusion Criteria

  • •Anything that prevents a subject from having isovolemic hemodilution

Outcomes

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Joseph D. Tobias

Chairman Dept. of Anesthesiology & Pain Medicine

Nationwide Children's Hospital

Study Sites (1)

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