- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06726733
Assessing Intensive Care Unit (ICU) Indications: Human vs. ChatGPT-4o Predictions (ICU)
Evaluation of the Accuracy of Intensive Care Unit (ICU) Admission Indications in Emergency Department Patients: A Comparison Between Clinical Decisions and ChatGPT-4o Prediction
Study Overview
Status
Detailed Description
This study has a retrospective design. The medical data of patients admitted to the emergency department and consulted to the anesthesiology and reanimation clinic for ICU indications will be collected retrospectively. Demographic information, vital signs, laboratory results, imaging findings, and clinical decisions of the patients will be recorded. These data will be systematically collected for each patient using an individual Case Report Form.
Inclusion Criteria for the Study:
Patients aged 18 years and older who were consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department will be included in the study.
Exclusion Criteria for the Study:
Patients consulted to the anesthesiology and reanimation clinic for ICU indications from inpatient services.
Patients consulted to the anesthesiology and reanimation clinic from the emergency department for reasons other than ICU indications.
Patients consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department but with insufficient recorded data (patients with data loss).
Model Training and Prediction Analysis:
ChatGPT-4 will be trained according to the guidelines in "Yoğun Bakım Hasta Kabul Kriterleri (Rehberleri)" by Çiftçi B, Erdoğan C, and Demiraran Y (5). The collected patient data will be presented to the ChatGPT-4 model to obtain predictions regarding whether the patients require ICU admission. The predictions made by ChatGPT will be compared with clinical decisions, and accuracy rate, false positive rate, and false negative rate will be analyzed.
Statistical Analysis Methods to Be Used in the Study:
Accuracy Rate: The rate at which ChatGPT correctly predicts ICU indications will be calculated.
False Positive Rate: The rate at which ChatGPT predicts ICU need for patients who do not require ICU admission will be evaluated.
False Negative Rate: The rate at which ChatGPT predicts no ICU need for patients who require ICU admission will be analyzed.
Kappa Statistics: The agreement between ChatGPT predictions and clinical decisions will be measured.
ROC Curve and AUC: The performance of ChatGPT will be evaluated using the ROC curve and AUC.
The Case Report Form used for each patient ensures detailed and systematic data collection of clinical information, aiming to meaningfully compare the alignment of ChatGPT's predictions with clinical decisions.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Bursa, Turkey (Türkiye)
- Bursa Yuksek Ihtisas Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients aged 18 years and older who are consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department will be included in the study.
Exclusion Criteria:
- Patients consulted to the anesthesiology and reanimation clinic for ICU indications from inpatient services.
- Patients consulted to the anesthesiology and reanimation clinic from the emergency department for reasons other than ICU indications.
- Patients consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department but with insufficient recorded data (patients with data loss)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Accuracy rate of ChatGPT-4 in predicting ICU indications
Time Frame: 3 month
|
3 month
|
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False positive rate
Time Frame: 3 month
|
3 month
|
|
False negative rate
Time Frame: 3 month
|
3 month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Kappa statistic
Time Frame: 3 month
|
3 month
|
Collaborators and Investigators
Investigators
- Principal Investigator: İlkay Ceylan, ceylanilkay@yahoo.com
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- BYIEAH-INKA
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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