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

Starting soon · Not applicable

Conditions studied: Temperature Monitoring

In brief

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

Key facts

Study ID: NCT07507396
Run by: Medical College of Wisconsin
People needed: 20
Starts: 2026-05-01
Expected to finish: 2027-05-01
Last updated by the study team: 2026-04-02

Who can join

Age: any, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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.
Patient has adequate forehead space to accommodate the TTP sensor
Temporal artery perfusion not compromised by injury or other pathology
No surgical procedure planned for 72 hours
Targeted temperature management expected for at least 24 hours at time of consent

You may not qualify if…

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.
A history of skin irritation, skin sensitivity, or skin disease, including psoriasis, eczema, atopic dermatitis, and skin cancer.
Pregnant or lactating female

Where it is running

Children's Wisconsin — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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