Non-invasive Temperature Monitoring in Pediatric Intensive Care Patients Requiring Targeted Temperature Management: Evaluation of Temple Touch Pro

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age0-17
SponsorMedical College of Wisconsin

About this trial

The purpose of this study is to evaluate the Temple Touch Pro (TTP) in Pediatric Intensive Care Unity (PICU) patients requiring targeted temperature control.

Eligibility criteria

Qualifiers

Age 0 to less than 18 years of age

PICU Diagnosis requiring targeted temperature management. For example traumatic brain injury, cardiac arrest, or anoxic brain injury

Requires continuous temperature monitoring with a foley catheter (bladder) or a general purpose probe placed in the esophagus.

Enrolled within 24 hours of start of continuous temperature monitoring.

Disqualifiers

Already enrolled in another trial addressing temperature management

Allergy to medical grade acrylic adhesive

Patient does not tolerate placement of TTP sensor on forehead

Contraindication to the placement of two or more of Foley, esophageal, and rectal temperature probes.

Trial design

Treatments tested in this trial

  • Temple Touch Pro

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

Medical College of Wisconsin

Lead sponsor

DeRoyal Industries, Inc.

Collaborator