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

KD
Overseen ByKayla Duvall, MD
Age: < 18
Sex: Any
Trial Phase: Academic
Sponsor: Medical College of Wisconsin
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of 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.

Are You a Good Fit for This Trial?

Inclusion Criteria

1. Age 0 to less than 18 years of age
2. PICU Diagnosis requiring targeted temperature management. For example traumatic brain injury, cardiac arrest, or anoxic brain injury
3. Requires continuous temperature monitoring with a foley catheter (bladder) or a general purpose probe placed in the esophagus.
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What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

1

Treatment groups

Active Control

Group I: Temple Touch ProActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Medical College of Wisconsin

Lead Sponsor

Trials
645
Recruited
1,180,000+

DeRoyal Industries, Inc.

Industry Sponsor

Trials
6
Recruited
750+