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Clinical Trials in China / NCT07382375
Starting soon Not applicable

AI-assisted Subtyping-directed Precision Treatment in Acute Aortic Dissection

NCT07382375 · tracked via the Priya Life Science China tracker
Sponsor
Nanjing Medical University
Phase
Not applicable
Started
2027-12-31
Last updated
2026-02-02

Condition(s) studied

Aortic Aneurysm and Dissection

Investigational drug(s) / intervention(s)

Ulinastatin and ThymalfasinUlinastatin →

Ulinastatin and Thymalfasin: AI-assisted Immunoinflammatory Subtyping-guided Target-matching Individualized Anti-inflammatory Strategy

Ulinastatin: Conventional empirical regimens will be formulated based on patients' clinical symptoms and routine inflammatory indicators (white blood cell count, C-reactive protein, procalcitonin) without uniform target-matching standards, with reference to clinical diagnosis and treatment guidelines: if obvious inflammatory responses are present (e.g., fever, significant elevation of C-reactive protein), non-steroidal anti-inflammatory drugs or low-dose glucocorticoids will be administered; if complicated with infection, combined antibiotic therapy will be given; for patients with normal or slightly elevated inflammatory indicators, anti-inflammatory drugs may be temporarily withheld, and close monitoring will be performed instead. The regimen will be adjusted according to changes in routine inflammatory indicators after surgery until the patient is discharged.

Study summary

Aortic dissection has acute onset and high mortality, with immunoinflammatory response driving lesion progression. Current perioperative anti-inflammatory therapies are mostly empirical and poorly targeted, and AI-assisted typing lacks a complete clinical translation pathway. This study integrates multi-dimensional data to construct an AI immunoinflammatory subtyping system, enabling rapid subtyping and establishing a "subtyping-target-treatment" closed loop for emergency needs. Using a prospective multicenter RCT, 300 patients are randomly divided into two groups: the experimental group receives subtyping-based precision therapy, while the control group uses empirical strategies (treatment of physician's choice). It observes 7-day postoperative SOFA score, SIRS and other prognostic indicators to provide evidence-based support for precision treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Confirmed diagnosis of acute aortic dissection by contrast-enhanced Computed Tomography Angiography (CTA) or Magnetic Resonance Angiography (MRA); 2. Planned emergency surgical treatment (including open surgery and endovascular repair); 3. Aged 18-80 years old, regardless of gender; 4. Time from onset to hospital admission ≤ 72 hours; 5. Signed informed consent form by the patient or their authorized agent, with willingness to cooperate with the follow-up of the study. Exclusion Criteria: 1. Complicated with underlying diseases that affect immunoinflammatory status, such as severe infections (e.g., sepsis, infective endocarditis), autoimmune diseases, malignant tumors, chronic liver diseases, and chronic kidney diseases (uremic stage); 2. Long-term use of immunosuppressants or glucocorticoids before surgery (continuous use for ≥ 2 weeks); 3. Pregnant or lactating women; 4. Patients with mental disorders or cognitive dysfunction who cannot cooperate with the study.

Primary outcome measure(s)

Trial sites (8)

FacilityCityRegionStatus
Beijing Anzhen Hospital Beijing China
Changzhou First People Hospital Changzhou China
West China Hospital of Sichuan University Chengdu China
Fujian Medical University Union Hospital Fuzhou China
The First Affiliated Hospital of Guangzhou Medical University Guangzhou China
Nanchang University Second Hospital Nanchang China
The First Affiliated Hospital of Nanjing Medical University Nanjing China
Shanghai East Hospital Shanghai China

More Nanjing Medical University trials in China

Other trials for the same condition

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 NCT07382375 on ClinicalTrials.gov ↗ ← All trials in China