Artifical IntelligenceASANCT07459491
AI vs. Anesthesiologists in Preoperative Triage
An observational study of Artifical Intelligence and Preoperative Evaluation, run by Damla Kaytancı Özçelik at 1 site in Turkey (Türkiye).
Trial summary
Accurate preoperative risk stratification is essential for perioperative planning, resource allocation, and patient safety. The American Society of Anesthesiologists Physical Status (ASA-PS) classification remains the most widely used global system for assessing preoperative health status. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Artifical Intelligence, Preoperative Evaluation
- How many people
- 703 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 10 Jan 2026to 1 May 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adult patients (≥18 years) scheduled for elective surgery and evaluated at the preoperative anesthesia outpatient clinic of Antalya City Hospital during the study period will constitute the study population. All eligible patients with a completed standardized preoperative anesthesia assessment form and documented ASA Physical Status classification will be considered. Only patients whose clinical data can be fully anonymized and who provide written informed consent will be included. Patients undergoing emergency surgery, pediatric patients, pregnant patients, ASA VI classification, incomplete documentation, or cases with more than 30 days between preoperative assessment and surgery will be excluded.
Who may be able to join
- Age ≥ 18 years
- Scheduled for elective surgery
- Completed standardized preoperative anesthesia evaluation form
- ASA Physical Status classification assigned by a specialist anesthesiologist
- Written informed consent
- Clinical documentation suitable for anonymization
Who cannot join
- Emergency surgery
- ASA VI classification
- Pregnancy
- Pediatric patients (<18 years)
- Incomplete or non-standardized clinical documentation
- Inability to anonymize clinical records
- More than 30 days between preoperative assessment and surgery
Trial locations and contacts
1 site in 1 country.
About this study
Official title: From Guideline-Based Risk Stratification To Dynamic Blood Resource Prediction: A Prospective Comparison Of Chatgpt-5 And Specialist Anesthesiologists İn Preoperative Assessment
Accurate preoperative risk stratification is essential for perioperative planning, resource allocation, and patient safety. The American Society of Anesthesiologists Physical Status (ASA-PS) classification remains the most widely used global system for assessing preoperative health status. However, ASA classification relies on clinician judgment and may demonstrate inter-observer variability.
Recent advances in artificial intelligence (AI), particularly large language models (LLMs), have shown potential for assisting clinical decision-making by synthesizing structured and unstructured medical information. In perioperative medicine, AI systems may support more standardized risk assessment and laboratory testing strategies.
Read more
The objective of this observational study is to evaluate the agreement between ASA classifications assigned by anesthesiologists and those generated by a large language model (ChatGPT-5) using anonymized preoperative clinical information. The study will also examine differences in laboratory test recommendations and explore the relationship between clinician- and AI-generated risk assessments and perioperative erythrocyte suspension utilization.
Adult patients scheduled for elective surgery who undergo routine preoperative anesthesia assessment will be included. For each patient, the ASA classification assigned by the anesthesiologist will be recorded and compared with the classification generated by the AI system using the same anonymized clinical information.
This study aims to assess whether AI-assisted preoperative evaluation may support more consistent risk stratification and potentially contribute to more standardized perioperative resource utilization.
Read the detailed description
Background and Rationale Preoperative risk assessment is a fundamental component of perioperative medicine and plays a central role in anesthetic planning, patient safety, and perioperative resource allocation. The American Society of Anesthesiologists Physical Status (ASA-PS) classification system remains the most widely used global method for describing preoperative health status. Despite its widespread adoption, ASA classification depends on clinician interpretation and may vary between evaluators.
Advances in artificial intelligence (AI), particularly large language models (LLMs), have introduced new opportunities for supporting clinical decision-making. These systems can process both structured and unstructured clinical information and may assist in standardizing certain medical classification tasks. In perioperative medicine, AI-assisted evaluation may help interpret patient comorbidities and clinical information in a consistent manner.
Another important component of preoperative assessment is laboratory test utilization. Preoperative laboratory testing is commonly used to identify potential perioperative risks; however, the number and type of tests ordered may vary among clinicians and institutions. AI-based systems may provide standardized recommendations for laboratory investigations and potentially contribute to more efficient resource utilization.
In addition, perioperative erythrocyte suspension (packed red blood cell, PRBC) transfusion represents an objective indicator of surgical physiological stress and perioperative resource use. Evaluating the relationship between risk classification and actual blood product utilization may help determine whether AI-assisted risk assessment has potential clinical relevance.
Study Design and Procedures This study is designed as a single-center observational study conducted at the preoperative anesthesia outpatient clinic of Antalya City Hospital. Adult patients undergoing routine preoperative anesthesia assessment before elective surgery during the study period will be included in the analysis.
For each patient, the ASA Physical Status classification assigned by the evaluating anesthesiologist during routine clinical care will be recorded. An anonymized summary of the same preoperative clinical information will then be analyzed by the artificial intelligence system (ChatGPT-5), which will generate an independent ASA classification.
The study will also compare laboratory test recommendations generated by the AI system with those ordered by anesthesiologists during routine preoperative evaluation. The number and types of laboratory tests recommended by each source will be recorded for comparison.
Information regarding perioperative erythrocyte suspension transfusion will be obtained from hospital electronic medical records. These data will be used to explore the relationship between risk classification and actual blood product utilization.
All clinical information used in the analysis will be anonymized before being processed by the AI system. AI outputs will not influence patient care or clinical decision-making.
Study Significance By comparing clinician-based and AI-generated preoperative assessments, this study aims to explore the potential role of large language models in supporting standardized risk stratification and resource utilization in anesthesia practice. The results may contribute to understanding whether AI-assisted evaluation can provide reliable support for preoperative clinical assessment.
- Conditions
- Artifical Intelligence, Preoperative Evaluation
- Being tested
- No intervention (observational study)
- Keywords
- artifical intelligence, chatgpt, anesthesia, Risk stratification, Perioperative medicine, preoperative assessment, Perioperative outcomes, Agreement analysis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
No intervention (observational study)Other
This is a non-interventional observational study. No therapeutic or diagnostic intervention is performed as part of the study
What is being measured
The primary outcome is the main question the study is designed to answer.
Agreement Between Anesthesiologist-Assigned and ChatGPT-5-Generated ASA Physical Status Classification
Agreement between ASA Physical Status classifications assigned by board-certified anesthesiologists and those generated by ChatGPT-5 using anonymized preoperative clinical data. Agreement will be quantified using Cohen's kappa and weighted kappa statistics for ordinal ASA categories (I-V). The comparison will be performed using identical anonymized preoperative clinical summaries.
Measured: At the time of preoperative anesthesia assessment (baseline).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Mar 2026
- Study start10 Jan 2026
- Primary completion10 Feb 2026
- Study completion1 May 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Artifical IntelligenceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 703 participants (actual)
Sponsor and investigators
- Lead sponsor
- Damla Kaytancı Özçelik
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Damla Kaytancı Özçelik, Antalya City Hospital
- Investigators
- Damla Kaytancı Özçelik, Principal investigator, Antalya City Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07459491
- Sponsor's protocol ID
- Antalya City Hospital
- Acronym
- ASA
- Status last verified
- Apr 2026
- First submitted
- 2 Mar 2026
- Last updated
- 2 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 2 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- From Guideline-Based Risk Stratification To Dynamic Blood Resource Prediction: A Prospective Comparison Of Chatgpt-5 And Specialist Anesthesiologists İn Preoperative Assessment
- ClinicalTrials.gov ID
- NCT07459491
- Acronym / sponsor ID
- ASA / Antalya City Hospital
- Conditions
- Artifical Intelligence, Preoperative Evaluation
- Keywords
- artifical intelligence, chatgpt, anesthesia, Risk stratification, Perioperative medicine, preoperative assessment, Perioperative outcomes, Agreement analysis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 703 participants (actual)
- Lead sponsor
- Damla Kaytancı ÖzçelikUniversity, hospital or other
- Study start
- 10 Jan 2026 (actual)
- Primary completion
- 10 Feb 2026 (actual)
- Study completion
- 1 May 2026 (actual)
- First posted
- 9 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Accurate preoperative risk stratification is essential for perioperative planning, resource allocation, and patient safety. The American Society of Anesthesiologists Physical Status (ASA-PS) classification remains the most widely used global system for assessing preoperative health status. However, ASA classification relies on clinician judgment and may demonstrate inter-observer variability.
Recent advances in artificial intelligence (AI), particularly large language models (LLMs), have shown potential for assisting clinical decision-making by synthesizing structured and unstructured medical information. In perioperative medicine, AI systems may support more standardized risk assessment and laboratory testing strategies.
The objective of this observational study is to evaluate the agreement between ASA classifications assigned by anesthesiologists and those generated by a large language model (ChatGPT-5) using anonymized preoperative clinical information. The study will also examine differences in laboratory test recommendations and explore the relationship between clinician- and AI-generated risk assessments and perioperative erythrocyte suspension utilization.
Adult patients scheduled for elective surgery who undergo routine preoperative anesthesia assessment will be included. For each patient, the ASA classification assigned by the anesthesiologist will be recorded and compared with the classification generated by the AI system using the same anonymized clinical information.
This study aims to assess whether AI-assisted preoperative evaluation may support more consistent risk stratification and potentially contribute to more standardized perioperative resource utilization.
Detailed description
Background and Rationale Preoperative risk assessment is a fundamental component of perioperative medicine and plays a central role in anesthetic planning, patient safety, and perioperative resource allocation. The American Society of Anesthesiologists Physical Status (ASA-PS) classification system remains the most widely used global method for describing preoperative health status. Despite its widespread adoption, ASA classification depends on clinician interpretation and may vary between evaluators.
Advances in artificial intelligence (AI), particularly large language models (LLMs), have introduced new opportunities for supporting clinical decision-making. These systems can process both structured and unstructured clinical information and may assist in standardizing certain medical classification tasks. In perioperative medicine, AI-assisted evaluation may help interpret patient comorbidities and clinical information in a consistent manner.
Another important component of preoperative assessment is laboratory test utilization. Preoperative laboratory testing is commonly used to identify potential perioperative risks; however, the number and type of tests ordered may vary among clinicians and institutions. AI-based systems may provide standardized recommendations for laboratory investigations and potentially contribute to more efficient resource utilization.
In addition, perioperative erythrocyte suspension (packed red blood cell, PRBC) transfusion represents an objective indicator of surgical physiological stress and perioperative resource use. Evaluating the relationship between risk classification and actual blood product utilization may help determine whether AI-assisted risk assessment has potential clinical relevance.
Study Design and Procedures This study is designed as a single-center observational study conducted at the preoperative anesthesia outpatient clinic of Antalya City Hospital. Adult patients undergoing routine preoperative anesthesia assessment before elective surgery during the study period will be included in the analysis.
For each patient, the ASA Physical Status classification assigned by the evaluating anesthesiologist during routine clinical care will be recorded. An anonymized summary of the same preoperative clinical information will then be analyzed by the artificial intelligence system (ChatGPT-5), which will generate an independent ASA classification.
The study will also compare laboratory test recommendations generated by the AI system with those ordered by anesthesiologists during routine preoperative evaluation. The number and types of laboratory tests recommended by each source will be recorded for comparison.
Information regarding perioperative erythrocyte suspension transfusion will be obtained from hospital electronic medical records. These data will be used to explore the relationship between risk classification and actual blood product utilization.
All clinical information used in the analysis will be anonymized before being processed by the AI system. AI outputs will not influence patient care or clinical decision-making.
Study Significance By comparing clinician-based and AI-generated preoperative assessments, this study aims to explore the potential role of large language models in supporting standardized risk stratification and resource utilization in anesthesia practice. The results may contribute to understanding whether AI-assisted evaluation can provide reliable support for preoperative clinical assessment.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients (≥18 years) scheduled for elective surgery and evaluated at the preoperative anesthesia outpatient clinic of Antalya City Hospital during the study period will constitute the study population. All eligible patients with a completed standardized preoperative anesthesia assessment form and documented ASA Physical Status classification will be considered. Only patients whose clinical data can be fully anonymized and who provide written informed consent will be included. Patients undergoing emergency surgery, pediatric patients, pregnant patients, ASA VI classification, incomplete documentation, or cases with more than 30 days between preoperative assessment and surgery will be excluded.
Key inclusion criteria (6 listed)
- Age ≥ 18 years
- Scheduled for elective surgery
- Completed standardized preoperative anesthesia evaluation form
- ASA Physical Status classification assigned by a specialist anesthesiologist
- Written informed consent
Key exclusion criteria (7 listed)
- Emergency surgery
- ASA VI classification
- Pregnancy
- Pediatric patients (<18 years)
- Incomplete or non-standardized clinical documentation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No intervention (observational study)This is a non-interventional observational study. No therapeutic or diagnostic intervention is performed as part of the study | Other | – |
Primary outcome
Agreement Between Anesthesiologist-Assigned and ChatGPT-5-Generated ASA Physical Status Classification
Time frame: At the time of preoperative anesthesia assessment (baseline).
Agreement between ASA Physical Status classifications assigned by board-certified anesthesiologists and those generated by ChatGPT-5 using anonymized preoperative clinical data. Agreement will be quantified using Cohen's kappa and weighted kappa statistics for ordinal ASA categories (I-V). The comparison will be performed using identical anonymized preoperative clinical summaries.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Jul 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Damla Kaytancı Özçelik principal investigator
Antalya City Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Artifical Intelligence and Preoperative Evaluation, run by Damla Kaytancı Özçelik at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Agreement Between Anesthesiologist-Assigned and ChatGPT-5-Generated ASA Physical Status Classification (time frame: At the time of preoperative anesthesia assessment (baseline).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jul 2026.