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
Sponsors and collaborators
Medical College of Wisconsin
Lead sponsor
DeRoyal Industries, Inc.
Collaborator