Prospective AI-SC Trial
Liver Cirrhosis
De qué trata este estudio
El registro no identifica actualmente este estudio como reclutando. Consulta su estado antes de planificar una evaluación.
- Tipo de estudio
- Observacional
- Fase
- No aplica / no indicada
- Rango de edad
- 18 años - 70 años
- Sexo admitido
- Todos los sexos
- Voluntarios sanos
- No aceptados
- Participantes
- 200 Estimado
Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.
Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.
Acerca de la investigación
This is a prospective, pre-post implementation study designed to evaluate how artificial intelligence-based selection committee (AI-SC) recommendations affect decision-making when integrated into routine clinical workflows. The study will focus on individual liver transplant candidacy decisions as the primary unit of analysis. Researchers will observe and analyze these decisions during weekly University Health Network (UHN) Liver Transplant Selection Committee meetings over an approximate 12-month period. The goal is to determine if the deployment of AI-SC recommendations changes, optimizes, or influences the committee's final transplant candidacy determinations compared to baseline practices.
Leer la descripción completa
The study will be conducted over an approximate 12-month period during regular weekly UHN Liver Transplant Selection Committee meetings. The primary unit of analysis is the individual liver transplant candidacy decision. The AI-SC output is then presented as an advisory decision-support summary. The committee may maintain or modify its decision and/or rationale. The final decision remains the decision of the human committee.
The study utilizes a pre-post implementation design:
1. Pre-Implementation Phase (Baseline): The committee will conduct evaluations and reach candidacy decisions according to standard clinical workflows without access to the AI tool.
2. Post-Implementation Phase (Intervention): The committee will be presented with the AI-SC recommendations during their routine workflow before finalising the candidacy decision.
Objectives and Evaluated Metrics The primary objective is to evaluate the direct effect of AI-SC recommendations on committee decision-making when deployed prospectively.
To comprehensively assess this impact, the secondary objectives will systematically measure:
- Decision Dynamics: The frequency and specific direction of transplant candidacy decision changes (e.g., from deferral to approval, or vice versa) following the introduction of AI-SC reviews.
- Decision Quality and Rationale: The impact of the tool on the clinical rationale's quality, transparency, completeness, actionability, and perceived fairness.
- Clinician Factors: Multi-disciplinary team members' confidence, acceptance, trust, perceived usefulness, and the overall workflow burden imposed by the tool.
- Predictors of Influence: Patient- and case-specific characteristics that are statistically associated with AI-influenced decision changes.
- Algorithmic Fairness and Equity: The consistency and fairness of the AI tool across diverse patient demographics and clinical profiles, specifically examining sex, race, ethnicity, height, ABO blood group, liver disease etiology, and Area Deprivation Index (ADI).
- Operational Feasibility: System performance metrics including software uptime, error rates, and the tangible impact on weekly meeting duration.
- Clinical Insight and Safety Catchment: Documentation of instances where the AI-SC successfully flags missing clinical data, guideline-relevant issues, potential contraindications, or overlooked clinical opportunities that were not emphasized during the initial multi-disciplinary discussion.
Eligibility Criteria:
Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No
Inclusion Criteria:
- Age 18 years or older.
- Undergoing a liver transplant assessment at UHN.
- Anticipated presentation and discussion at the weekly UHN Liver Transplant Selection Committee meeting.
- Ability to provide informed consent.
Exclusion Criteria:
- Refusal or withdrawal of consent.
- Cases for which required committee presentation information is unavailable to the study team.
- Cases in which urgent clinical circumstances do not allow the informed consent process to occur prior to the scheduled committee review.
- Cases in which the treating clinical team determines that research contact is inappropriate due to severe clinical, emotional, or logistical circumstances.
¿Quién podría participar?
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Inclusion Criteria:
- age 18 years or older; undergoing liver transplant assessment at UHN; anticipated discussion at the UHN liver transplant selection committee; ability to provide informed consent
Exclusion Criteria:
- refusal or withdrawal of consent; cases for which required committee presentation information is unavailable to the study team; cases in which urgent clinical circumstances do not allow the consent process to occur before committee review; cases in which the treating team determines that research contact is inappropriate because of clinical, emotional, or logistical circumstances.
Refusal to participate will not affect transplant assessment, committee review, clinical management, waitlist eligibility, or access to future care.
Población del estudio
Adult patients with liver cirrhosis assessed for liver transplantation at UHN who may be presented at the weekly UHN Liver Transplant Selection Committee meeting.
Entiende la evaluación inicialTratamiento, grupos y participación
El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.
- Asignación
- No informado
- Enmascaramiento
- No informado
Artificial Intelligence Selection Committee (AI-SC) OTHER
The AI-SC is an investigational clinical decision-support tool designed to provide a structured advisory recommendation for liver transplant candidacy discussions. It consists of six specialty-specific LLM-based agents representing hepatology, transplant surgery, cardiology, anesthesiology, psychiatry, and social work. The system uses a retrieval-augmented generation framework that references a locked knowledge base of institutional transplant criteria and relevant clinical guidelines.
Qué evalúan los investigadores
Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.
Medidas principales
Frequency of modification of transplant committee decisions after presentation of the AI-SC recommendation, measured as the proportion of cases in which the final post-AI decision differs from the recorded initial pre-AI decision
Plazo: During weekly UHN Liver Transplant Selection Committee meetings for approximately 12 months.
No informado en este registro.
Revisa las tablas completas y sus limitaciones en el registro oficial.
Abrir resultados oficiales ↗Centros de investigación (1)
El estado general puede diferir del estado de un centro. Confirma la disponibilidad antes de trasladarte.
1 centros
Ajmera Transplant Centre, Toronto General Hospital, UHNToronto, Ontario, CanadaEstado desconocido
Equipo y fechas
- Patrocinador principal
- University Health Network, Toronto
- Inicio del estudio
- 13 nov 2026 Estimado
- Finalización primaria
- 2027-11 Estimado
- Finalización del estudio
- 2028-11 Estimado
- Primera publicación
- 10 nov 2026 Real
- Última actualización
- 10 nov 2026 Real
Contactos oficiales del estudio
Título oficial del estudio
Artificial Intelligence-Selection Committee (AI-SC) Trial: A Prospective Study of Human-AI Collaborative Decision-Making in Liver Transplant Selection
Consulta a Wellness Clinical Research
Tu mensaje va a WCR, incluso si otra organización realiza este estudio. WCR puede orientarte, pero podría no realizar este estudio, tener acceso a su equipo ni poder inscribirte.
Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.
Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026
