Evaluation of Accuracy of the Owlet OSS 3.0 Sensor in the Neonatal Population
Recruiting
N/A
Interventional Study
Pulse Oximeter Validation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 0 Days – 28 Days
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 20 (estimated)
- Sponsor
- Owlet Baby Care, Inc. · Industry
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About This Trial
The sponsor of this study, Owlet Baby Care, Inc., is comparing the accuracy of their pulse oximeter Sensor with the measurements of oxygen levels in newborns who are already being monitored with arterial blood samples. A minimum of 20, but up to 100 participants will be enrolled in a hospital environment and need to weigh 1500 grams or more. The purpose of the testing is to gather information on p…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Less than or equal to 44 weeks corrected gestational age
* Weight equal or greater than 1500g
* Subjects with standard of care (SOC) arterial blood sampling line already in place at time of enrollment, with anticipated arterial blood gas measurements as part of their plan of c…
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