AzTrials
AzTrials

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).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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.

Turkey (Türkiye)1 site
  • Antalya City Hospital

    Antalya

Other trials in Turkey (Türkiye)

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.

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.

  1. 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.

  1. First posted9 Mar 2026
  2. Study start10 Jan 2026
  3. Primary completion10 Feb 2026
  4. Study completion1 May 2026

Resources

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)
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

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.

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