- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06493175
The Application of Large Language Model in Emergency Chest Pain Triage (ALERT)
July 8, 2024 updated by: Tang Yida, Peking University Third Hospital
This study will evaluate the accuracy and efficiency of large language model in emergency triage.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The study is to evaluate the value of large language model in emergency triage, their accuracy and efficiency were evaluated and compared with traditional triage.
To explore whether the model can effectively reduce the workload of medical staff, while improving the speed and quality of triage.
In addition, the ability of the model to predict serious medical events such as acute heart events and strokes was evaluated.
It also included surveys of patients; acceptance and satisfaction with the use of the artificial intelligence-assisted triage system.
Analyze the economic benefits of adopting this technology, including cost saving and optimal allocation of resources.
Study Type
Interventional
Enrollment (Estimated)
2000
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xiangbin Meng
- Phone Number: 17600220171
- Email: puthxnk@126.com
Study Locations
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Beijing
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Beijing, Beijing, China
- Recruiting
- Peking University Third Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- All patients with chest pain entered the emergency triage procedure.
- patients aged 18 and above.
Exclusion Criteria:
- Patients with severe cognitive impairment or inability to communicate.
- There are patients who have been explicitly referred to specific departments (for example, some of the 120 transfer patients, who may go directly to the green channel) .
- Patients with unstable vital signs .
- Patients with potential medical problems.
- Is participating in other clinical trials.
- Failure to follow test procedures.
- Those who refuse to sign the informed consent form.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Large Language Model Diagnostic
Patients interacted with the large-language model triage system MedGuide-V5 during the waiting period before or after routine triage in the emergency department.
During this phase, MedGuide-V5 will automatically record data and metrics during communication with patients.
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The large language model MedGuide-V5 is able to quickly extract key information from a patients description, and by analyzing these descriptions, it provides physicians with a possible initial diagnosis to help them quickly prioritize the treatment of patients.
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|
Active Comparator: Routine diagnostic and therapeutic procedure
After the artificial intelligence system evaluation, the patients will receive the diagnosis and treatment according to the normal procedure.
The overall time of artificial triage, the triage of patients, and other data will be recorded.
Patient visits should not be delayed by the use of artificial intelligence systems for evaluation.
|
After the artificial intelligence system evaluation, the patients will receive the diagnosis and treatment according to the normal procedure.
The overall time of artificial triage, the triage of patients, and other data will be recorded.
Patient visits should not be delayed by the use of artificial intelligence systems for evaluation.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Diagnostic Accuracy Rate of MedGuide-V5
Time Frame: through study completion, an average of 10 months
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To assess the consistency of the diagnosis of chest pain made by physicians with the assistance of large language models with the actual diagnosis made by patients after all examinations were completed.
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through study completion, an average of 10 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Satisfaction of Medical Personnel
Time Frame: during evaluation
|
To evaluate the satisfaction and acceptance of medical personnel with the use of large language models in assisting triage systems through methods such as questionnaire surveys.
The name of this questionnaire is: Researcher Evaluation Form, with scores ranging from 1 to 10.
The higher the score, the more helpful the large language model is to researchers.
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during evaluation
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Medical Personnel Treatment Plan Adjustment Rate
Time Frame: during evaluation
|
The number of times medical personnel adjust treatment plans after receiving feedback from MedGuide V5's results and referring to the suggestions provided by the large language model.
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during evaluation
|
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Emergency Department Revisit Rate within 30 Days
Time Frame: during evaluation
|
Evaluate the occurrence of patients revisiting the emergency department or being readmitted within 30 days after large language model-assisted triage and traditional triage.
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during evaluation
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Yi-Da Tang, MD, PhD, Peking University Third Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 20, 2023
Primary Completion (Estimated)
December 20, 2024
Study Completion (Estimated)
December 20, 2024
Study Registration Dates
First Submitted
December 22, 2023
First Submitted That Met QC Criteria
July 8, 2024
First Posted (Actual)
July 9, 2024
Study Record Updates
Last Update Posted (Actual)
July 9, 2024
Last Update Submitted That Met QC Criteria
July 8, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- M2023828
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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