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Study identifier: NCT07170527 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Long-Term Outcomes and Post-Intensive Care Syndrome: Investigating the Associations Between Metabolic Signatures and Physical Functioning in Critically Ill Patients

Condition: Post-Intensive Care Syndrome (PICS)  ·  Sponsor: ARH van Zanten, MD PhD

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Despite being young, healthy, and physically fit, some intensive care unit (ICU) patients experience significantly worse functional recovery after critical illness than older patients with multiple comorbidities although a poor precondition seems to be associated with worse ICU outcomes. This paradox highlights a fundamental gap in our understanding of the determinants of long-term recovery. While nonmodifiable factors such as age and pre-existing disease explain part of the variation, they cannot fully account for the wide heterogeneity in outcomes. Metabolic disturbances during critical illness, such as hypercatabolism, impaired muscle metabolism, nutritional deficits, systemic inflammation, and disruption of gut health, are likely to influence recovery trajectories, yet remain poorly characterized. Because these processes represent potentially modifiable targets, combining their evaluation with nonmodifiable patient characteristics is essential for unraveling the complex, multifactorial mechanisms underlying post-intensive care syndrome (PICS). This explorative, prospective, observational study aims to investigate the associations between metabolic signatures during the acute phase of critical illness and PICS outcomes throughout the recovery trajectory of ICU survivors, with a primary focus on physical functioning. In addition, the study explores the longitudinal course of metabolic parameters from ICU admission up to 12 months post-discharge, and whether these signature…

This description comes directly from the study's public registry record.

Talk to the study team

Arthur HR van Zanten, MD, PhD  ·  +31318435964  ·  zantena@zgv.nl

Noortje MP Overwater, MSc  ·  +31318434119  ·  noverwater@zgv.nl

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Locations (1)

Gelderse Vallei HospitalEde, Gelderland, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT07170527