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ACTIVE NOT RECRUITING
NCT07459491

Agreement Between ChatGPT-5 and Anesthesiologists in Preoperative Risk Assessment: ASA Classification

Sponsor: Damla Kaytancı Özçelik

View on ClinicalTrials.gov

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. 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.

Official title: Evaluating Large Language Models for Preoperative Risk Stratification: ChatGPT-5 vs. Anesthesiologists on ASA Classification and Blood Transfusion Prediction

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

703

Start Date

2025-12-02

Completion Date

2026-05-01

Last Updated

2026-03-10

Healthy Volunteers

No

Interventions

OTHER

No intervention (observational study)

This is a non-interventional observational study. No therapeutic or diagnostic intervention is performed as part of the study

Locations (1)

Antalya City Hospital

Antalya, Turkey (Türkiye)