Artificial Intelligence: AI technology will provide novel imaging markers and generate a radiology report with relevant key slice imaging and evaluation results
Study summary
The CHinese pulmOnary Embolism Multimodality Imaging-artifiCial intelligencE Study (CHOICE) is a prospective observational multi-center study that will collect imaging text data and raw data of patients with pulmonary embolism (PE) in China. By combining artificial intelligence technology, it aims to identify imaging markers to assist in early diagnosis, differential diagnosis, risk stratification, and prognosis assessment of PE.
Eligibility
Sex
ALL
Min age
14 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* 14 Years and older
* Patients suspected of PE
Exclusion Criteria:
* Pregnant women
* Refuse to follow up
* Incomplete or discontinued imaging scans
* Insufficient quality of image data to allow for analysis
Primary outcome measure(s)
Diagnostic rate of PE — 2 years Comparison before and after AI technique.
APE risk stratification rates (low, intermediate low, intermediate high and high risk) — 2 years Comparison before and after AI technique.
Disease severity of chronic thromboembolic pulmonary disease (CTEPD)/chronic thromboembolic pulmonary hypertension (CTEPH) — 2 years Comparison before and after AI technique. Assessment of disease severity is comprehensive, referring to the comprehensive risk assessment in pulmonary arterial hypertension (three-strata model) \[DOI: 10.1183/13993003.00879-2022\], including clinical observations and modifiable variables. The higher the score, the more severe the condition.
30 day mortality — 2 years Patient mortality (death) at 30-days post-PE diagnosis. Comparison before and after AI technique.
Trial sites (1)
Facility
City
Region
Status
China-Japan Frendship hospital
Beijing
China
Recruiting
More China-Japan Friendship Hospital trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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