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Emergency Severity Scoring and Process Re-engineering for Type A Aortic Dissection

Emergency Severity Scoring and Process Re-engineering for Type A Aortic Dissection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109896
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Acute type A aortic dissection

Interventions

case series:NA

Sponsors

Beijing Anzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old, gender not limited; 2. Patients diagnosed with acute type A aortic dissection; 3. Understand the purpose of this trial and participate voluntarily, and sign the informed consent form

Exclusion criteria

Exclusion criteria: 1.Pregnant and lactating women; 2. Patients who are known to be allergic to the drug components used in the study; 3. Have received drugs or other intervention measures used in similar studies before; 4. There are other circumstances that may affect the research results or safety, which shall be ruled out by the researcher. 5. The researchers believe that it is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
The time from entering the emergency department to the start of the operation;

Secondary

MeasureTime frame
The incidence of preoperative complications (such as new-onset stroke, gastrointestinal bleeding, vascular rupture, myocardial infarction, etc.);Preoperative hemodynamic parameters and fluid input and output;Patient mortality rate;Health Economics;

Countries

China

Contacts

Public ContactYipping Ge

Beijing Anzhen Hospital. Capital Medical University

yipengge@126.com+86 135 8171 9652

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026