Trial on the Impact of Indirect Calorimetry-Guided Nutritional Support on Patient-Centered Outcomes in Critically Ill Patients - The OPTICal Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHEIDEGGER CP

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

356 Participants
are divided into 2 treatment groups

Sponsors and collaborators

HEIDEGGER CP

Lead sponsor

University Hospital, Geneva

Sponsor institution

University Hospital, Zürich

Collaborator

GHOL Nyon Hospital

Collaborator