Clinical Trial: Comparative Evaluation of smART+ REE Module to an FDA-cleared Device, for REE Calculation in ICU Patients

U.S., Sept. 11 -- ClinicalTrials.gov registry received information related to the study (NCT07165080) titled 'Comparative Evaluation of smART+ REE Module to an FDA-cleared Device, for REE Calculation in ICU Patients' on April 21.

Brief Summary: A prospective, single-center, comparative evaluation of smART+ REE Module to an FDA-cleared REE Module device, for REE calculation in ICU Patients.

Study Start Date: Aug. 12

Study Type: OBSERVATIONAL

Condition: Comparative Study REE Resting Energy Expenditure

Intervention: DEVICE: smART+ REE

The two study devices will be used simultaneously: the patient's respiratory equipment will be connected directly to the smART+ REE module, and then the COSMED Q-NRG+ will be connected just downstream of ...