Ireland
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Recruiting Observational

Chinese PE Multimodality Imaging Artificial Intelligence Study

NCT06526468 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2010-09-01
Last updated
2024-08-28

Condition(s) studied

Pulmonary EmbolismChronic Thromboembolic Pulmonary HypertensionChronic Thromboembolic Pulmonary Disease

Investigational drug(s) / intervention(s)

Artificial Intelligence

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)

FacilityCityRegionStatus
China-Japan Frendship hospital Beijing China Recruiting
Official registry record

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.

View NCT06526468 on ClinicalTrials.gov ↗ ← All trials in China