Evaluation of Pulse Oximetry Sensors in Neonates

TerminatedOBSERVATIONAL
Enrollment

32

Participants

Timeline

Start Date

September 30, 2005

Study Completion Date

May 31, 2010

Conditions
Premature Birth
Interventions
DEVICE

Adhesive and non-adhesive oximetry sensors

A sample of 32 premature infants will be recruited to participate in this study in which an adhesive sensor and a nonadhesive sensor are compared. Both sensors will be simultaneously tested in each subject, for a period of 14 days, with one sensor on the right foot and the other sensor on the left foot. Data will be collected on sensor longevity, skin integrity at the sensor site, reason for sensor replacement and ease of use rating by the clinician. Data will be summarized using descriptive statistics.

Trial Locations (1)

60611

Ann & Robert H Lurie Children's Hospital of Chicago, Chicago

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Medtronic - MITG

INDUSTRY

lead

Ann & Robert H Lurie Children's Hospital of Chicago

OTHER