ClinicalTrials.gg
Active, not recruitingNCT07885007Updated Oct 21, 2026

AI-SC Multi-center Study

An observational study in Liver Cirrhosis, sponsored by University Health Network, Toronto. Active, not recruiting at 1 site in Canada. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by University Health Network, Toronto · Observational

Updated Oct 21, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
1,000
Ages
18 Years to 70 Years
Sex
All
01

Study summary

To examined the opportunity for Artificial Intelligence (AI) agents to evaluate transplant candidacy objectively at LT-SC, with a large language models (LLM) representing the expertise of each individual specialist (hepatologist, surgeon, anesthesiologist, psychiatrist and social worker) and coming up with a group consensus decision upon inter-agent communication using prompts GPT-4 in OpenAI (private version).

Read the detailed description

The study seeks to evaluate the feasibility and acceptability of integrating such AI agents into LT candidate assessments with a retrospective evaluation and validation of a multi-disciplinary selection committee of AI agents (AI-SC) at major transplant centers, including MeDanTa (India), King Saud bin Abdulaziz University (Saudi Arabia), King Abdullah International Medical Research Center (Saudi Arabia), National University Hospital (Singapore), UCSF Health (US), Vanderbilt University Medical Center (US), John Hopkins Hospital (US), Mayo Clinic (US), Royal Prince Alfred Hospital (AU), and University Health Network (UHN-CA).

02

Conditions studied

  • Liver Cirrhosis

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Keywords

  • AI-SC Agent Multicenter
03

In context

Liver Cirrhosis

1,668 studies on the registry are indexed under Liver Cirrhosis; 360 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 152 across 605 observational studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

University Health Network, Toronto is the lead sponsor of 1,432 studies on the registry; 292 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 3 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

patient with liver cirrhosis on evaluation for liver transplant

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patient more or equal to 18 years of age with liver cirrhosis on assessment for liver transplant

Exclusion criteria

Exclusion Criteria:

  • multi-organ transplant
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
1,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • AI-SC

    AI - Selection Committee

    Other: evaluate the alignment between AI-SC recommendations and LT-SC decisions · Other: Multi AI-SC model

  • Human Liver transplant (LT)-SC

    Human Liver Transplant Selection Committee

Interventions

  • Otherevaluate the alignment between AI-SC recommendations and LT-SC decisions

    To validate the developed model, we invited other collaborating centers, including Vancouver Coastal Health (Canada), Mayo Clinic (US), John Hopkins Hospital (US), Royal Prince Alfred Hospital (AU), National University of Singapore (Singapore), UCSF Health (US), Vanderbilt University Medical Center (US), John Hopkins Hospital (US), MeDanTa (India), and Ministry of National Guard Health Affairs (Saudi Arabia) to perform a validation as an extension of data governance phase.

  • OtherMulti AI-SC model

    To evaluate the feasibility and acceptability of integrating such multi AI-SC(Selection Committee) agents into LT candidate assessments.

06

What researchers measure

Primary outcomes

  1. Concordance of AI-SC vs LT-SC review

    · Our primary outcome will be any substantial change in the content, method, or result of the patient assessment between the AI-SC and conventional reports. We will calculate the percentage of concordance between the two, and the similarity of report generated by the human and the AI-SC will be evaluated using ROUGE score (Recall-Oriented Understudy for Gisting Evaluation), a quantitative metric that assesses textual similarity3.

    Time frame: 3 months

  2. Concordance between AI-SC vs LT-SC

    Our primary outcome will be any substantial change in the content, method, or result of the patient assessment between the AI-SC and conventional reports. We will calculate the percentage of concordance between the two, and the similarity of report generated by the human and the AI-SC will be evaluated using ROUGE score (Recall-Oriented Understudy for Gisting Evaluation), a quantitative metric that assesses textual similarity3

    Time frame: 3 months

Secondary outcomes

  1. Time of adjudication

    • The secondary outcomes will be the safety of assessments in cases where substantial changes are made, time required for adjudications, frequency of decision changes between AI-SC and conventional LT-SC. We will also evaluate the consistency of the decision making across controversial variables, such as age, cardiovascular health, and frailty over time, to evaluate whether AI-SC can provide more objectivity in the decision-making.

    Time frame: 3 months

07

Study locations

1 site
  • Toronto General Hospital
    Toronto, Ontario M5G 2N2, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07885007
Collaborators
Mayo University Hospital, University of California, San Francisco, Vanderbilt University Medical Center, Johns Hopkins University, Medanta, The Medicity, India, Royal Prince Alfred Hospital, Sydney, Australia, National University Hospital, Singapore, King Saud Bin Abdulaziz University for Health Sciences
Responsible party
Sponsor
First posted
Oct 21, 2026
Start date
Apr 1, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 21, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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