About this trial
This multicentric randomized controlled trial aims to evaluate whether indirect calorimetry (IC)-guided nutritional support improves patient-centered outcomes in critically ill adult patients compared to standard formula-based nutritional strategies. The study includes mechanically ventilated patients expected to remain in the ICU for more than 72 hours. The intervention group will receive nutritional targets based on measured resting energy expenditure using the QNRG+ device, with a gradual escalation of energy delivery following current ESPEN guidelines. The primary outcome is quality of life at 3 months post-ICU admission, assessed using the EQ-5D-5L. Secondary outcomes include functional recovery, muscle preservation, infection rates, and rehospitalization. This study is the first to assess the long-term impact of IC-guided nutrition on recovery and quality of life using a patient-centered approach.
Eligibility criteria
Qualifiers
≥18 years old
On Mechanical Ventilation
Expected ICU length of stay >72 hours
Disqualifiers
Refusal of the family or patient
Patient transferred from another ICU
Pregnant patient
Patient is planned for a withdrawal of care or is actively dying
Trial design
Treatments tested in this trial
- Indirect Calorimetry Group
- Control Group - Formula-Based Group
Treatment groups
Sponsors and collaborators
HEIDEGGER CP
Lead sponsor
University Hospital, Geneva
Sponsor institution
University Hospital, Zürich
Collaborator
GHOL Nyon Hospital
Collaborator