PRotEin Provision in Critical IllneSs -2

NCT07529522 — Not applicable, Not yet recruiting, 1026 participants, Ziekenhuis Oost-Limburg

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The Impact of Low Versus Standard Enteral Protein Provision on Health-related Quality of Life Following Intensive Care Admission: a Randomised Controlled, Multicentre, Parallel Group Trial in Mechanically Ventilated, Critically Ill Patients

RegistryNCT07529522, acronym PRECISe-2
StatusNot yet recruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: triple, other
Enrollment1026 (Estimated)
SponsorZiekenhuis Oost-Limburg (Other); collaborators: Federaal Kenniscentrum voor Gezondheidszorg, Belgium
ConditionsCritical Illness, Intensive Care (ICU)
Interventionsenteral nutrition (Other)
Datesstart 2026-09-01 (estimated), primary completion 2029-07-01 (estimated), completion 2029-07-01 (estimated), first posted 2026-04-14, last updated 2026-09-09
Locations15 sites in Belgium, Netherlands

Related Papers Related Patents Related Grants Related Experts
All trials for Critical Illness All trials for Intensive Care (ICU) All trials of enteral nutrition

-Summary

When patients survive a life-threatening condition in the intensive care unit (ICU), they often face a prolonged recovery process marked by persistent health issues that significantly reduce their quality of life. Muscle weakness is the most defining feature of this post-intensive care syndrome. This weakness, along with the associated decline in quality of life, presents major challenges for patients, their families, and the healthcare system, including the high costs of long-term care.

Until recently, it was believed that providing additional nutrition-particularly protein-during the early phase of a critical illness could help prevent muscle loss and promote recovery. However, the recent PRECISe study showed that administering a high amount of protein (target: 2 g/kg per day) via feeding tube actually worsened outcomes: patients who received high-protein nutrition during the acute phase reported a lower quality of life over the six months following ICU admission and were discharged from the hospital later.

These findings from the PRECISe study have renewed attention on the amount of protein administered to critically ill patients. Current European ICU nutrition guidelines (1.3 g/kg per day) recommend a higher protein intake than the daily recommended amount for healthy individuals (0.8 g/kg per day). However, in critically ill patients, protein metabolism may be impaired, potentially leading to the accumulation of toxic protein breakdown products and hindering recovery, ultimately resulting in a lower quality of life.

Reducing protein intake below the level recommended for healthy individuals during the acute phase of a life-threatening illness-while maintaining total energy intake (calories)-may be beneficial for long-term recovery and rehabilitation.

The PRECISe-2 study investigates whether patients who receive less protein (0.6-0.8 g/kg per day) but sufficient energy during the early phase of their critical illness feel better and experience a higher quality of life in the long term compared to those who receive the standard amount of protein (1.3 g/kg per day).

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+Arms and interventions

ArmTypeInterventionsDescription
Low protein enteral feeding formulaExperimentalOther: enteral nutrition
Standard protein enteral feeding formulaActive comparatorOther: enteral nutrition
  • enteral nutrition (Other): 0.6 g protein/kg per day during the first 10 days of enteral nutrition and thereafter 0.8 g protein/kg per day
  • enteral nutrition (Other): 1.3 g protein/kg per day during the entire treatment duration

+Outcome measures

Primary outcomes

  • overall longitudinal between group-difference in Health-Related Quality of Life (HRQL) at 30, 60, and 90 days after index ICU admission corrected for the pre-admission EQ-5D-5L summary index, assessed by EuroQoL (EQ-5D-5L) [30, 60, and 90 days after index ICU admission]

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Adult (≥ 18 years-old) patient
* Admission to the ICU
* Invasive, mechanical ventilation initiated within 72 hours following ICU admission, or mechanically ventilated upon arrival to the ICU
* Expected ICU stay on mechanical ventilation of ≥ 3 days after randomisation

Exclusion Criteria:

* Expected contra-indication for enteral nutrition for at least one week, at the discretion of the treating physician, such as a bowel discontinuity that cannot be solved within one week
* Moribund (expected to die within 48 hours) or withholding of treatment (DNR code 3)
* Previous inclusion in the PRECISe-2 trial
* Transfer from another ICU with an ICU stay longer than 3 days

+Locations (15)

FacilityCityCountryStatus
UZ AntwerpenAntwerpBelgium
Ziekenhuis Oost-LimburgGenkBelgium
AZ Maria MiddelaresGhentBelgium
UZ GentGhentBelgium
Jessa ZiekenhuisHasseltBelgium
UZ BrusselJetteBelgium
AZ GroeningeKortrijkBelgium
UZ LeuvenLeuvenBelgium
UZ LeuvenLeuvenBelgium
CHC MontLégiaLiègeBelgium
CHR de la CitadelleLiègeBelgium
CHU LiègeLiègeBelgium
Clinique St. PierreOttignies-Louvain-la-NeuveBelgium
AZ DeltaRoeselareBelgium
MUMC+MaastrichtNetherlands