Performance of Pulse Oximeter Sensors in Neonates

NCT03870373 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2021-04-01

No results posted yet for this study

Summary

Validate pulse oximeter sensors in neonates by comparing sensor readings to blood samples during cardiac surgery.

Conditions

  • Cardiac Surgery

Interventions

DEVICE

Pulse Oximeter

Aulisa's non-invasive pulse oximeter sensor is applied to a foot of the neonate; an adhesive patch secures the sensor to the neonate.

Sponsors & Collaborators

Principal Investigators

  • Hung G Nguyen, MD · UCSF Medical Center at Mission Bay

Eligibility

Min Age
0 Days
Max Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-01
Primary Completion
2019-05-05
Completion
2019-05-10
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03870373 on ClinicalTrials.gov