Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 31 of 620 for:    oximeter

Masimo CO-Oximeter Study

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01184521
Recruitment Status : Completed
First Posted : August 19, 2010
Last Update Posted : January 31, 2012
Sponsor:
Information provided by (Responsible Party):
Joseph D. Tobias, Nationwide Children's Hospital

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.

Condition or disease
Cardiac Surgical Procedures

Layout table for study information
Study Type : Observational
Actual Enrollment : 50 participants
Observational Model: Case Control
Time Perspective: Prospective
Official Title: Use of the Masimo Rainbow SET Pulse CO-Oximeter in Patients Undergoing Isovolemic Hemodilution
Study Start Date : September 2010
Actual Primary Completion Date : July 2011
Actual Study Completion Date : July 2011

Group/Cohort
pulse CO-oximeter



Primary Outcome Measures :
  1. hemoglobin value [ Time Frame: 1 Day (day of surgery) ]
    The accuracy of the hemoglobin value from the Masimo pulse oximeter during isovolemic hemodilution.



Information from the National Library of Medicine

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, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients requiring isovolemic hemodilution during surgery.
Criteria

Inclusion Criteria:

  • Any subject that is scheduled to have isovolemic hemodilution

Exclusion Criteria:

  • Anything that prevents a subject from having isovolemic hemodilution

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01184521


Locations
Layout table for location information
United States, Ohio
Nationwide Children's Hospital
Columbus, Ohio, United States, 43147
Sponsors and Collaborators
Nationwide Children's Hospital

Layout table for additonal information
Responsible Party: Joseph D. Tobias, Chairman Dept. of Anesthesiology & Pain Medicine, Nationwide Children's Hospital
ClinicalTrials.gov Identifier: NCT01184521     History of Changes
Other Study ID Numbers: IRB10-00364
First Posted: August 19, 2010    Key Record Dates
Last Update Posted: January 31, 2012
Last Verified: January 2012