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NCT05992506

Electroencephalographic Biomarker to Predict Postoperative Delirium

Active, enrolled Last updated 20 November 2025
What this trial tests

trial testing POD risk estimation using PEUMA in Postoperative Delirium in 264 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 September 2023
Primary endpoint
31 October 2025
30 June 2026

Quick facts

Lead sponsorUniversity of Chile
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment264
Start date1 September 2023
Primary completion31 October 2025
Estimated completion30 June 2026
Sites2 locations across Chile

Drugs / interventions tested

Conditions studied

Sponsor

University of Chile

Who can join

Adults 60 to 100, any sex, with Postoperative Delirium. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Acute post-operatory cognitive dysfunction states are one of the most important complications in older patients that underwent surgery. Among them postoperative delirium (POD) is the the most studied. Patients who develop delirium have poorer long-term outcomes, such as longer length of hospital stay, institutionalization at discharge, and even higher mortality, and consequently, the human and economic costs significantly increase for the health system. Here the research team will use an observational cohort, investigator blinded in five-center with a primary endpoint to validate intraoperative EEG analysis as a reliable biomarker of postoperative delirium.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Postoperative Delirium

Currently open trials in the same condition.

Other University of Chile trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05992506.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing