Clinical Trials in the USA / NCT07168798
Enrolling by invitation
Observational
SpO2 Accuracy in Children
NCT07168798 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Hypoxemia
Investigational drug(s) / intervention(s)
Pulse oximeter
Pulse oximeter: OLV-4201 pulse oximeter with sensors: TL-272T3, TL-274T3 and TL-273T3
Study summary
Evaluation of SpO2 Accuracy in Children with Various Skin Color
Eligibility
Inclusion Criteria:
* Children aged 0 - 12 who are admitted to the CICU with or plan to have an indwelling arterial line for standard care
Exclusion Criteria:
* Patients with elevated levels of methemoglobin and carboxyhemoglobin, or anemia.
* Patients with prolonged hypotension at the time of enrollment.
* Patients with ductal-dependent congenital cardiac disease.
Primary outcome measure(s)
- SpO2 accuracy — 24 hours
Evaluate the accuracy of Nihon Kohden SpO2 in measuring blood oxygen levels in children with varying skin tones
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Childrens Hospital of Philadelphia | Philadelphia | Pennsylvania |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07168798 on ClinicalTrials.gov ↗ ← All trials in the USA