NCT07783334

Brief Summary

This prospective observational study evaluates the performance of artificial intelligence (AI) models in preoperative anesthesia assessment. Preoperative clinical data from adult patients undergoing elective surgery are independently evaluated by clinicians and AI models (ChatGPT and Gemini). The study compares their assessments of American Society of Anesthesiologists (ASA) physical status classification and the predicted need for intensive care unit (ICU) admission within the first 24 hours after surgery. Actual postoperative ICU admission is used as the clinical outcome for evaluating predictive performance. No treatment or clinical decision is determined by the AI models, and patient management is performed according to routine clinical practice.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 16, 2026

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

August 20, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 20, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 24, 2026

Completed
Last Updated

August 24, 2026

Status Verified

August 1, 2026

Enrollment Period

6 months

First QC Date

August 20, 2026

Last Update Submit

August 20, 2026

Conditions

Keywords

artificial intteligencepreoperative assessmentASA physical status classificationIntensive Care Unit admissionChatGPTGeminiAnesthesiology

Outcome Measures

Primary Outcomes (1)

  • Agreement in ASA Physical Status Classification

    Agreement between clinician-assigned and AI-generated ASA Physical Status classifications will be evaluated for ChatGPT and Gemini using linear weighted kappa statistics.

    During preoperative assessment

Secondary Outcomes (1)

  • Prediction of Postoperative ICU Admission

    Within the first 24 hours after surgery

Study Arms (1)

elective surgical patients

Adult patients undergoing elective surgery who undergo routine preoperative anesthesia assessment. Preoperative clinical data from each participant are independently evaluated by the clinician and the AI models ChatGPT and Gemini for ASA physical status classification and prediction of ICU admission within the first 24 postoperative hours. AI assessments do not influence clinical management or patient care.

Other: AI-assisted preoperative assesment

Interventions

Preoperative clinical data are independently evaluated using ChatGPT and Gemini for ASA physical status classification and prediction of ICU admission within 24 hours after surgery. AI-generated assessments are used for research purposes only and do not influence clinical decision-making or patient care.

elective surgical patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients undergoing elective surgery who are evaluated in the preoperative anesthesia clinic at Bakirkoy Dr. Sadi Konuk Research and Training Hospital.

You may qualify if:

  • Age 18 years or older
  • Scheduled for elective surgery
  • Evaluated in the preoperative anesthesia clinic
  • Provision of informed consent

You may not qualify if:

  • Pregnancy
  • Presence of an upper respiratory tract infection
  • Active herpes infection or active wound and/or lesion in the anesthesia-related area
  • Age under 18 years
  • Emergency surgery
  • Planned cardiovascular surgery
  • Incomplete clinical data

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bakırköy Dr. Sadi Konuk Training and Research Hospital

Istanbul, Istanbul, 34147, Turkey (Türkiye)

Location

Study Officials

  • evrim kucur tülübaş, MD

    Bakirkoy Dr. Sadi Konuk Research and Training Hospital

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
anesthesiology and reanimation resident

Study Record Dates

First Submitted

August 20, 2026

First Posted

August 24, 2026

Study Start

February 16, 2026

Primary Completion

August 20, 2026

Study Completion

August 20, 2026

Last Updated

August 24, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared due to patient confidentiality and data protection considerations.

Locations