- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05497258
IDEAS-AAP System Diagnoses Acute Abdominal Pain
Computer-aided, Evidence-based System Improved Clinical Diagnostic Accuracy of Certificated-Physicians in Acute Abdominal Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430060
- Renmin Hospital of Wuhan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Males or females who are over 18 years old;
- After qualified medical education and obtained the Certificate of medical practitioner;
Exclusion Criteria:
- Physicians without qualified medical education and didn't obtain the Certificate of medical practitioner;
- The researcher believes that the subjects are not suitable for participating in clinical trials.
Study Plan
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: Experimental: with Artificial intelligence assistant system
The physicians were additionally provided with the feature extracted by the system, a list of suspicious diagnoses predicted by IDEAS-AAP, and corresponding diagnostic criteria according to guidelines. After the readers get the examination results, the IDEAS-AAP will renew its diagnosis prediction. IDEAS-AAP extracted feature from electronic health record, provided a list of suspicious diagnoses, and corresponding diagnostic criteria according to guidelines. After the readers get the examination results, the IDEAS-AAP will renew its diagnosis prediction. |
The AI-assisted diagnosis system can provide the direction of disease diagnosis in real time and assist the doctor to give the final diagnosis
|
|
No Intervention: No Intervention: without Artificial intelligence assistant system
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The accuracy of clinical diagnosis.
Time Frame: one week
|
Calculation method = number of right cases / total number of cases 100%
|
one week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of the prediction of disease based on whole electronic health record
Time Frame: one week
|
Calculation method = number of right cases / total number of cases 100%
|
one week
|
|
The prediction of disease based on whole electronic health record and criteria matching
Time Frame: one week
|
Calculation method = number of right cases / total number of cases 100%
|
one week
|
|
Time cost of EHR reading
Time Frame: one week
|
one week
|
Collaborators and Investigators
Investigators
- Principal Investigator: Honggang Yu, MD, Renmin Hospital of Wuhan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022K-K146(C01)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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