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Establishing a New Strategy of Risk Stratification of Acute Aortic Intramural Hematoma Using Radiomics Combined with Machine Learning

Establishing a New Strategy of Risk Stratification of Acute Aortic Intramural Hematoma Using Radiomics Combined with Machine Learning

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120919
Enrollment
Unknown
Registered
2026-03-23
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

aortic intramural hematoma (IMH)

Interventions

Observation group:None

Sponsors

ZhongShan Hospital Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Meet all the following criteria: 1. Age >=18 years; 2. Intramural aortic hematoma thickness >5 mm; 3. Hemodynamically stable at presentation, with no indications for emergency surgery; 4. Informed consent has been obtained; 5. Acute onset <=14 days, diagnosed as a Stanford Type B intramural aortic hematoma;

Exclusion criteria

Exclusion criteria: Meet any one of the following criteria: 1.Initial CTA at presentation shows involvement of the ascending aorta; 2. Complex IMH presenting with hemodynamic instability at initial presentation, requiring urgent surgical intervention; Diagnostic criteria for complex IMH are based on the 2024 ESC guidelines and include meeting any one of the following: (1) Aortic rupture; (2) Symptoms of visceral, lower extremity, or spinal cord ischemia; (3) Periaortic hematoma; (4) Rapid enlargement of the aortic diameter; (5)Recurrent pain or uncontrolled hypertension despite optimal medical therapy; 3. Concurrent connective tissue disease, such as Marfan syndrome; 4. Rheumatic or immunological disorders involving the aorta; 5. History of aortic disease treated with aortic endovascular stent graft implantation; 6. Severe cardiac, pulmonary, or hepatic failure; 7. Severe renal failure (creatinine > 250 µmol/L) not on dialysis; 8. History of active malignant tumors; 9. Life expectancy of less than 1 year; 10. Inability to undergo or tolerate CTA examinations during follow-up due to factors such as contrast agent allergy; 11. Requirement for long-term oral anticoagulants (e.g., warfarin) due to other medical conditions; 12. Women of childbearing potential who have tested negative for pregnancy but refuse to use effective contraception, or women who are pregnant or breastfeeding; 13. Participation in or ongoing enrollment in a clinical trial of a drug or medical device within the past 30 days; 14. History of severe drug or alcohol abuse within the past year; 15. Conditions deemed unsuitable for participation in this study by the investigators, such as mental illness, cognitive or emotional disorders that prevent understanding or compliance with the study.

Design outcomes

Primary

MeasureTime frame
aoritc adverse events;

Countries

China

Contacts

Public ContactDong Zhihui

ZhongShan Hospital Fudan University

dzh926@126.com+86 135 6424 9168

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026