- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06494748
Evaluating the Efficacy of Artificial Intelligence Models in Predicting Intensive Care Unit Admission Needs
Study Overview
Detailed Description
Intensive care units (ICUs) are critical components of healthcare systems, providing life-saving care to patients with severe and life-threatening conditions. Timely and accurate prediction of ICU admission needs is essential for improving patient outcomes and optimizing hospital resource allocation. Delayed ICU admissions have been consistently associated with higher morbidity and mortality rates. With the advent of artificial intelligence (AI) in healthcare, there is an opportunity to enhance clinical decision-making by leveraging AI models to predict ICU needs accurately. AI models, such as ChatGPT and Gemini, can process vast amounts of complex data to identify patterns that might not be immediately evident to human clinicians, potentially improving the speed and accuracy of ICU admission decisions.
This is an observational retrospective study. Data were collected from electronic health records (EHRs) from a hospital retrospectively.
Data were extracted from EHRs and included:
Demographic data: Age, gender, and basic patient characteristics. Clinical parameters: Medication information, consultation details, ECG findings, imaging results, comorbid conditions (e.g., diabetes mellitus, hypertension, heart failure, COPD, cerebrovascular events), and laboratory values (e.g., hemoglobin, hematocrit, platelet count, PT, INR, procalcitonin, ALT, AST, bilirubin, sodium, potassium, chloride, glucose, creatinine, urea, albumin, thyroid function tests).
Prediction data: AI model predictions and actual ICU admission decisions.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 34303
- Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients over the age of 18
- Patients consulted for anesthesia regarding intensive care needs
- Patients with sufficient data in the hospital's electronic health record system
Exclusion Criteria:
- Patients with insufficient data in the hospital records
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Anesthesiologists Decision
Intensive Care Unit Follow up need is decided by anesthesiologists.
|
0: No need to follow up in Intensive Care Unit 1: Need to follow up in Intensive Care Unit |
|
Artificial Intelligence Decision
Intensive Care Unit Follow up need is decided by Artificial Intelligence
|
0: No need to follow up in Intensive Care Unit 1: Need to follow up in Intensive Care Unit |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intensive Care Unit Need
Time Frame: 1 day
|
The primary outcome measure of this study is the accuracy of the predictions made by the artificial intelligence (AI) models, ChatGPT and Gemini, regarding the need for ICU admissions.
This will be evaluated by comparing the AI model predictions to the actual clinical decisions made regarding ICU admissions.
|
1 day
|
Collaborators and Investigators
Investigators
- Principal Investigator: Engin ihsan Turan, Specialist, Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ICU-retro
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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