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A multicenter clinical study on the early diagnostic value of bedside detection of soluble growth-stimulating expression gene 2 protein (sST2) in acute aortic dissection

A multicenter clinical study on the early diagnostic value of bedside detection of soluble growth-stimulating expression gene 2 protein (sST2) in acute aortic dissection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116910
Enrollment
Unknown
Registered
2026-01-16
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Acute aortic dissection

Interventions

Gold Standard:The gold standard: Use CTA to show "aortic intimal tear and true or false lumen formation" or the dissection rupture under direct vision during surgery as the basis for the diagnosis of
Index test:soluble suppression of tumorigenicity 2, sST2

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old, with the onset time of "acute chest pain" (sudden pain in the chest, back, abdomen, etc.) <=24 hours and visiting the emergency department; 2. Clinically suspected AAD (tearing pain, bilateral blood pressure asymmetry, abnormal pulse, shock and other signs, or imaging suggesting aortic widening, etc.); 3. All completed the detection of sST2, D-dimer, troponin, brain natriuretic peptide and aortic Computed tomography angiography (CTA) examination; 4. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The time from the onset of the disease to seeking medical attention is more than 24 hours; 2. Combined with other known diseases that affect sST2 levels; Such as acute and chronic heart failure, fulminant myocarditis, etc. 3. The sample is hemolyzed, lipemic or collected improperly; 4. The patient has a history of immune deficiency diseases (such as HIV, etc.), or a history of cancer, malignant tumors, or autoimmune diseases, or severe cardiovascular and cerebrovascular diseases, or other diseases that may significantly reduce life expectancy; 5. Have any medical history that may affect compliance with the protocol (such as severe mental disorders, cognitive dysfunction, drug abuse or addiction, etc.); 6. Pregnant or lactating women, or those who are fertile but unwilling or unable to take effective contraceptive measures; 7. Patients who the researcher determined were not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
soluble suppression of tumorigenicity 2;Whole aortic CTA;Troponin;Brain natriuretic peptide;

Secondary

MeasureTime frame
D-Dimer;

Countries

China

Contacts

Public ContactHu Bei

Guangdong Provincial People's Hospital

qhubei@hotmail.com+86 159 1869 3156

Outcome results

None listed

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