Comparing Validity of Non-Invasive Hemoglobin Monitoring to Laboratory Results in Critically Ill Children

Completed

Conditions studied: Hemoglobin Results

In brief

This is a prospective study to determine the accuracy of the Masimo Pronto Non-Invasive Hemoglobin Monitor and associated Rainbow® probes in the detection of hemoglobin concentration in critically ill children.

Key facts

Study ID

NCT01750463

Run by

University of North Carolina, Chapel Hill

People needed

65

Starts

2013-01-01

Expected to finish

2013-05-01

Last updated by the study team

2014-12-03

Who can join

Age: 0 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient has been admitted to Pediatric Intensive Care Unit
• Patient age is ≥ 30 days old and ≤ 18 years old
• Patient weight ≥ 3 Kg.
• Patient requires hemoglobin monitoring

You may not qualify if…

• Patient does not have exposed fingers/toes,due to congenital anomalies wound dressing or injury.
• Patient weight is less than 3 Kg
• Patient is less than 30 days old

Where it is running

• Pediatric Intensive Care Unit, University of North Carolina — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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