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Study identifier: NCT05331118 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Perioperative Longitudinal Study of Complications and Long-term Outcomes

Condition: Perioperative Complication · Infections · Myocardium; Injury  ·  Sponsor: UMC Utrecht

PhaseN/A
Planned participants9000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Purpose: with an increased risk of complications. Improved preoperative risk stratification and earlier diagnosis of these complications may ameliorate postoperative recovery and improve long-term outcomes. The perioperative longitudinal study of complications and long-term outcomes (PLUTO) aims to establish a comprehensive biorepository that will facilitate research in this field. Patients undergoing elective intermediate to high-risk non-cardiac surgery are eligible for enrolment. For the first 7 postoperative days (or longer as indicated), participants will be subjected to daily bedside visits by dedicated observers, who adjudicate clinical events and perform non-invasive physiological measurements (including handheld spirometry and single-channel EEG). In addition, we will collect blood samples as well as microbiome specimens at selected time points. Primary study outcomes are the postoperative occurrence of nosocomial infections, major adverse cardiac events, pulmonary complications, acute kidney injury and delirium. Secondary outcomes include mortality as well as long-term psychopathology, cognitive dysfunction, and quality of life. PLUTO is the first perioperative biobank worldwide that includes a broad range of high-risk surgical patients, collecting prospective bedside data as well as both blood and microbiome specimens during the entire perioperative period. The data and materials collected in PLUTO will be used to develop, externally validate, and update prognost…

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

Talk to the study team

Nikki de Mul, MSc  ·  +31887561124  ·  PLUTO@umcutrecht.nl

Always discuss trial participation with your own doctor first.

Locations (1)

University Medical Center UtrechtUtrecht, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT05331118