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

NCT07165080 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2025-11-18

No results posted yet for this study

Summary

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

Conditions

  • Comparative Study
  • REE
  • Resting Energy Expenditure

Interventions

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 that. See the diagram and key below:

Sponsors & Collaborators

  • ART Medical Ltd.

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-12
Primary Completion
2025-10-21
Completion
2025-10-30
FDA Device
Yes

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07165080 on ClinicalTrials.gov