NCT07395791

Brief Summary

Accurate prediction of postoperative intensive care unit (ICU) requirement is essential for patient safety and efficient use of limited ICU resources. In routine clinical practice, decisions regarding postoperative ICU admission are primarily based on anesthesiologists' preoperative clinical judgment, which may vary among clinicians. This prospective, observational study aims to evaluate the agreement between predictions made by ChatGPT-5(Chat Generative Pre-trained Transformer) and anesthesiologists regarding postoperative ICU requirement using routinely collected preoperative patient data, and to compare these predictions with actual postoperative ICU admission outcomes. The study does not involve any intervention, treatment modification, or additional procedures beyond standard clinical care. All patient data are anonymized, and clinical management is not influenced by the model's predictions

Trial Health

75
On Track

Trial Health Score

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

Enrollment
938

participants targeted

Target at P75+ for all trials

Timeline
0mo left

Started Dec 2025

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 Progress95%
Dec 2025Jun 2026

Study Start

First participant enrolled

December 7, 2025

Completed
24 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

February 1, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

February 11, 2026

Status Verified

January 1, 2026

Enrollment Period

24 days

First QC Date

February 1, 2026

Last Update Submit

February 7, 2026

Conditions

Keywords

Artificial IntelligenceChatGPTAnesthesiologyIntensive Care UnitPostoperative CareRisk Prediction

Outcome Measures

Primary Outcomes (1)

  • Agreement Between Predicted and Actual Postoperative ICU Requirement

    Agreement between preoperative predictions of postoperative intensive care unit (ICU) requirement made by ChatGPT-5 and anesthesiologists, compared with actual postoperative ICU admission outcomes.

    Within the first 24 hours after surgery

Interventions

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

Eligibility Criteria

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

The study population consists of adult patients aged 18 years and older who underwent elective surgical procedures and received preoperative anesthesiology evaluation at a tertiary care hospital. The study includes patients for whom postoperative intensive care unit (ICU) requirement was assessed based on preoperative clinical data. Patient outcomes were evaluated according to actual postoperative ICU admission status.

You may qualify if:

  • Adult patients aged 18 years or older.
  • Patients undergoing elective surgical procedures requiring preoperative anesthesiology evaluation.
  • Availability of complete preoperative clinical data required for postoperative intensive care unit (ICU) need prediction.
  • Patients evaluated preoperatively by an anesthesiology specialist.

You may not qualify if:

  • Patients younger than 18 years of age.
  • Emergency surgical procedures.
  • Patients with incomplete or missing preoperative clinical data.
  • Patients who decline the use of their clinical data for research purposes.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Antalya City Hospital

Antalya, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Observation

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Beste Mutlu Dağlıoğlu

    Antalya City Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Specialist in Anesthesiology and Reanimation

Study Record Dates

First Submitted

February 1, 2026

First Posted

February 9, 2026

Study Start

December 7, 2025

Primary Completion

December 31, 2025

Study Completion (Estimated)

June 1, 2026

Last Updated

February 11, 2026

Record last verified: 2026-01

Locations