Pulse Oximetry_Performance Testing- PCBA-1 (Printed Circuit Board Assembly) NEO/PEDS
Completed
Conditions studied: Subjects With an Existing Intra-arterial Line
In brief
To determine accuracy specifications of the pulse oximeter in the NEO/PEDS subject population
Key facts
- Study ID
- NCT01797250
- Run by
- Medtronic - MITG
- People needed
- 12
- Starts
- 2013-05-01
- Expected to finish
- 2013-07-01
- Last updated by the study team
- 2013-12-06
Who can join
Age: 0 and older, up to 18. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subject or legal guardian is willing and able to sign informed consent prior to study initiation.
- Subject is able to participate for the duration of the evaluation. In most instances, the length of the study will not exceed twenty-four hours.
- Subject satisfies a specified sensor requirement (see Table 1).
- Requires use of an intra-arterial line for medical reasons such as continuous blood pressure monitoring or frequent arterial blood draws.
- Subject is able to accommodate multiple sensors.
- Neonatal subjects up to 1 month of age or Pediatric subjects 1 month up to 18 years old.
You may not qualify if…
- Subjects that have an existing health condition, in which the investigators determine that safe or accurate oximetry measures may not be obtained at the areas where the pulse oximetry sensor could be placed, will not be included in the study. For example, anyone with burns, abrasions or surface lesions on the contact areas would be excluded.
- Any subject whose treatment or condition would be compromised if they were to participate in this study and any patient whose use of a pulse oximeter and sensor would present a potential for serious risk to health, safety, or welfare.
- Subject has severe contact allergies that may react to standard adhesive materials found in pulse oximetry sensors.
- Subject cannot be reliably monitored with a pulse oximeter as a result of inadequate pulsatile signals.
- Subject has had a procedure using injected intravascular dyes within 24 hours preceding testing
Where it is running
- Children's Hospital- Los Angeles — Los Angeles, California, United States
- Wasatch Neonatal — Orem, Utah, United States
Full record on ClinicalTrials.gov
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