Trial reportJPEN. Journal of parenteral and enteral nutrition2026
Combined intravenous bolus amino acid supplementation and mobilization on early muscle loss in critically ill adults: A randomized controlled trial.
Trial report in JPEN. Journal of parenteral and enteral nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
8 citing papers in PubMed.
- Combined intravenous bolus amino acid supplementation and mobilization on early muscle loss in critically ill adults: A randomized controlled trial.JPEN. Journal of parenteral and enteral nutrition · 2026Trial
- Personalized protein delivery in critical care: from phenotyping and endotyping to post-ICU recovery.Current opinion in critical care · 2026Review
- Reply to "Mechanical tension and autophagy suppression: Unmasking the confounders in ICU muscle preservation strategies".JPEN. Journal of parenteral and enteral nutrition · 2026Article
- Timing-specific neutrality in a rigorous ICU anabolic trial.JPEN. Journal of parenteral and enteral nutrition · 2026Article
- Reply to: Timing-specific neutrality in a Rigorous ICU anabolic trial.JPEN. Journal of parenteral and enteral nutrition · 2026Article
- Mechanical tension and autophagy suppression: Unmasking the confounders in ICU muscle preservation strategies.JPEN. Journal of parenteral and enteral nutrition · 2026Article
- Body composition-guided protein dosing in critically ill patients: a before-and-after study (PROGRESS-ICU).Critical care (London, England) · 2026Observational
- Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
backgroundMuscle wasting is a hallmark of critical illness. We evaluated the effect of amino acid supplementation and mobilization on early muscle loss in critically ill patients.
methodsWe conducted a randomized parallel-group trial involving adult patients admitted to the surgical intensive care unit of a tertiary hospital. Participants were randomly assigned to two groups, both receiving standard care nutrition and mobilization. The intervention group also received a daily intravenous amino acid bolus with 45 min of cycle ergometry, starting on days 3-4 for a mean of 6 days. The primary co-outcomes were changes in vastus lateralis myofiber cross-sectional area (from biopsies) and ultrasound-derived rectus femoris cross-sectional area, measured between the preintervention (day 2) and postintervention (day 8) time points. Analyses were conducted using mixed-model analysis of variance and least significant difference testing. Secondary outcomes included the protein-to-DNA ratio, muscle echogenicity, whole-body phase angle, muscle strength (Medical Research Council sum score) and physical capability (6-min walk test).
resultsFifty patients (90% male, age 37 ± 12 years) were included. Standard of care participants received 1.23 ± 0.18 g/kg/day protein; intervention participants 1.57 ± 0.27 g/kg/day, including 0.37 ± 0.05 g/kg/day from the supplement. Muscle loss occurred significantly over time (biopsy P = 0.01; ultrasound P < 0.001), with no significant differences between groups. Similarly, no significant differences were observed in protein-to-DNA ratio, muscle echogenicity, phase angle, muscle strength, or physical capability.
conclusionA short-duration combined intervention of intravenous bolus amino acids and cycle ergometry, limited to the acute phase of critical illness, did not reduce muscle loss or improve muscle quality, strength, or physical capability.
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Registered trials
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