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Protein Dosing Strategies in Critically Ill Patients:

Protein Dosing Strategies in Critically Ill Patients: Comparing Actual Body Weight and Fat-Free Mass Approaches in an Observational Cohort Study - Protein intake ICU patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58270
Enrollment
620
Registered
2025-10-22
Start date
2025-10-26
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical illness Critical illness

Interventions

One group of patients received proteins based on ABW (Actual Body Weight) until July 2023, and a second group was based on FFM (Fat-Free Mass). No intervention, only standard care.&nbsp

Sponsors

Ziekenhuis Gelderse Vallei
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients meeting all of the following criteria are eligible for the study: 1. Age = 18 years 2. A BIA measurement within 48 hours after ICU admission 3. Two BIA measurements during ICU stay

Exclusion criteria

Exclusion criteria: Any patient meeting one or more of the following criteria is not eligible for the study: 1. Transfer from another ICU resulting in the first BIA measurement >48 hours after admission to Gelderse Vallei Hospital 2. A previous ICU admission within 2 weeks before the current admission 3. Contra-indications for BIA measurement: i. Patients with electrical implants such as a pacemaker or ICD ii. Patients who cannot maintain posture for the (5 min) duration of the measurement iii. Patients with wounds or skin damage in the designated electrode sight iv. Pregnancy

Design outcomes

Primary

MeasureTime frame
Primary: The primary outcome measure of this study is mortality, comparing patients who received protein based on actual body weight with those who received protein based on fat-free mass. Mortality will be assessed as both short-term mortality (ICU and 30-day mortality) and long-term mortality (90-day mortality).

Secondary

MeasureTime frame
Secondary: Secondary outcome measures include several clinical and nutritional endpoints, all comparing the cohort receiving protein based on actual body weight with the cohort receiving protein based on fatfree mass: • ICU and hospital length of stay, defined as the total duration of ICU and hospital admission in days, measured from ICU admission until discharge. • Duration of invasive mechanical ventilation (IMV), defined as the number of days a patient receives IMV from initiation until discontinuation. • Urea–creatinine ratio (UCR) during ICU stay, comparing differences in UCR between both groups throughout the ICU stay. • Changes in BIA parameters over time, including changes in fat-free mass and other body composition measures, based on repeated bioelectrical impedance analysis (BIA) measurements during ICU stay. • Protein and energy intake during ICU stay, comparing daily and cumulative (first 14 days) protein and energy intake between the two groups.

Countries

Netherlands

Contacts

Public ContactMC Paulus

Ziekenhuis Gelderse Vallei

wetenschapsbureau@zgv.nl+318434119

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026