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Comparison of Delirium Evaluation Tools Effectiveness in Intensive Care Patients

NCT03934645 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2020-03-11

No results posted yet for this study

Summary

This study compares the efficacy of scoring models used in delirium prediction in patients applying to intensive care unit. The diagnosis of delirium is based on the Intensive Care Delirium Screening Checklist (ICDSC). The aim of this study is determine the sensitivity and specificity of three prediction models (Delirium prediction model for ICU patients version 1 \[Predeliric version-1\], Delirium prediction model for ICU patients version 2 \[Predeliric version-2\] and Early prediction model for delirium in ICU patients \[E-Predeliric\]).

Conditions

  • Delirium

Interventions

OTHER

Delirium prediction model for ICU patients, version 1

The pre-deliric model version 1 for intensive care patients consists of ten risk factors that are readily available within 24 hours after intensive care admission and has a high predictive value. The model allows for early prediction of delirium and initiation of preventive measures. Data of the patient in the first 24 hours of admission to the intensive care unit are collected and the delirium prediction score is found.

OTHER

Delirium prediction model for ICU patients, version 2

The pre-deliric model version 2 for intensive care patients consists of ten risk factors that are readily available within 24 hours after intensive care admission. Data of the patient in the first 24 hours of admission to the intensive care unit are collected and the delirium prediction score is found. The model allows for early prediction of delirium and initiation of preventive measures.

OTHER

Early prediction model for delirium in ICU patients

The e-pre-deliric model enables the clinician to identify those patients likely to develop delirium following ICU admission using only nine predictors. In the e-pre-deliric model, delirium prediction score is determined by inputting the data of the patient in admission to the intensive care unit.

Sponsors & Collaborators

  • Trakya University

    lead OTHER

Principal Investigators

  • DİLEK MEMİŞ, Proffesor · Trakya University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2019-06-30
Completion
2019-11-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03934645 on ClinicalTrials.gov