- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06321445
The Success of ChatGPT in Providing American Society of Anesthesiologist (ASA) Scores (ASA)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients of all ages and sexes with ASA scores ranging from I to IV who applied to the anesthesia clinics of Health Science University Istanbul Kanuni Sultan Suleyman Training and Research Hospital and Basaksehir Cam and Sakura City Hospital were included in the study. Patients with ASA scores of V and VI were not included in the study as their statistical distribution would be disrupted.
Data Collection Data were collected daily from preoperative examination evaluation forms in this study, which included Patient's Age Patient's Gender Patient's Weight Patient's Height Additional Illnesses Medications Used Abnormal Laboratory Findings Abnormal Imaging Findings Operation to be Performed Consultation Notes Given ASA Score ChatGPT's ASA Score. At Health Science University Istanbul Kanuni Sultan Suleyman Training and Research Hospita, the patient will be under the care of Specialist Doctor Engin İhsan Turan, and at Basaksehir Cam and Sakura City Hospital, under the care of Specialist Doctor Abdurrahman Engin Baydemir.
The natural language processing module ChatGPT 4, developed by OpenAI, was consulted for providing ASA scores based on the collected data. In addition to the collected data, ASA scores given by anesthesia experts were also entered into the system.
The investigators chose ChatGPT-4 among artificial intelligence models for our study due to its extensive use in the literature.
Primary Objective: To evaluate the success of ChatGPT-4 in predicting postoperative intensive care needs and mortality in adult patients with ASA scores of III and IV. Secondary Objectives: To examine the effectiveness of ChatGPT-4's recommendations on anesthesia methods and additional suggestions in the clinical decision-making process.
Benefits: Understanding the contributions of artificial intelligence-based systems to clinical decision-making processes.
Risks: The potential for ChatGPT-4's recommendations to be misleading, but the risk will be mitigated by doctors being the final decision-makers.
Use of ChatGPT 4 After the data mentioned above regarding the patients were transmitted to ChatGPT 4, ChatGPT 4 was asked to predict the ASA scores of the patients. To do so the investigators will create a special GPT which can provide ASA scores according to the newest guidelines. This GPT will assign patients an ASA score based on abnormal data while recognizing that the patients' other results and physical examination findings are normal.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Istanbul, Turkey, 34303
- Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient who admitted to anesthesia clinics for both hospital
- Patient with ASA scores between I-IV
Exclusion Criteria:
- ASA scores higher than IV
- Emergency cases patients have symptoms like upper and lower airway infections.
- patients haven't got enough informations to provide ASA scores.
- Patients with symptoms of an active upper or lower respiratory tract infection
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Experts
ASA scores provided by anesthesiologists
|
ASA scoring, or the American Society of Anesthesiologists (ASA) Physical Status Classification System, is a framework used by anesthesiologists to assess the preoperative physical fitness of a patient before surgery.
It categorizes patients into six classes based on their overall health status, ranging from ASA I (a healthy patient) to ASA VI (a declared brain-dead patient whose organs are being removed for donor purposes).
The ASA score helps in predicting perioperative risks and assists healthcare professionals in making informed decisions about anesthesia management and the need for special precautions during and after surgery.
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ChatGpt
ASA scores provided by ChatGpt
|
ASA scoring, or the American Society of Anesthesiologists (ASA) Physical Status Classification System, is a framework used by anesthesiologists to assess the preoperative physical fitness of a patient before surgery.
It categorizes patients into six classes based on their overall health status, ranging from ASA I (a healthy patient) to ASA VI (a declared brain-dead patient whose organs are being removed for donor purposes).
The ASA score helps in predicting perioperative risks and assists healthcare professionals in making informed decisions about anesthesia management and the need for special precautions during and after surgery.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Success of ChatGPT in Providing American Society of Anesthesiologist (ASA) Scores
Time Frame: 2 weeks
|
Comparison of ASA scores provided from ChatGpt and provided from anesthesiologists. ASA 1: A normal healthy patient. ASA 2: A patient with mild systemic disease. ASA 3: A patient with severe systemic disease that is not incapacitating. ASA 4: A patient with severe systemic disease that is a constant threat to life. ASA 5: A moribund patient who is not expected to survive without the operation. ASA 6: A declared brain-dead patient whose organs are being removed for donor purposes. Additional classifications include: E: This designation can be added to any of the above classifications (ASA 1E to ASA 6E) to indicate that the surgery is an emergency, which increases the risk of the procedure. |
2 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The Success of ChatGPT in clinical decisions
Time Frame: 2 weeks
|
Comparison of ASA scores provided from ChatGpt and provided from anesthesiologists. ASA 1: A normal healthy patient. ASA 2: A patient with mild systemic disease. ASA 3: A patient with severe systemic disease that is not incapacitating. ASA 4: A patient with severe systemic disease that is a constant threat to life. ASA 5: A moribund patient who is not expected to survive without the operation. ASA 6: A declared brain-dead patient whose organs are being removed for donor purposes. Additional classifications include: E: This designation can be added to any of the above classifications (ASA 1E to ASA 6E) to indicate that the surgery is an emergency, which increases the risk of the procedure. |
2 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Engin ihsan Turan, Specialist, Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
Publications and helpful links
General Publications
- Yeo YH, Samaan JS, Ng WH, Ting PS, Trivedi H, Vipani A, Ayoub W, Yang JD, Liran O, Spiegel B, Kuo A. Assessing the performance of ChatGPT in answering questions regarding cirrhosis and hepatocellular carcinoma. Clin Mol Hepatol. 2023 Jul;29(3):721-732. doi: 10.3350/cmh.2023.0089. Epub 2023 Mar 22.
- Wongtangman K, Aasman B, Garg S, Witt AS, Harandi AA, Azimaraghi O, Mirhaji P, Soby S, Anand P, Himes CP, Smith RV, Santer P, Freda J, Eikermann M, Ramaswamy P. Development and validation of a machine learning ASA-score to identify candidates for comprehensive preoperative screening and risk stratification. J Clin Anesth. 2023 Aug;87:111103. doi: 10.1016/j.jclinane.2023.111103. Epub 2023 Mar 8.
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
Other Study ID Numbers
- ChatGptASAscore
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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