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Expression Profiling of Adhesion Molecules in Thrombosis-Related Disorders

Expression Profiling of Adhesion Molecules in Thrombosis-Related Disorders

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114636
Enrollment
Unknown
Registered
2025-12-16
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Myocardial infarction, cerebral infarction, or lower limb arterial or venous thrombosis

Interventions

Gold Standard:Myocardial Infarction : Meet the diagnostic criteria established by theWHOor theACC/AHA. Cerebral Infarction: CTorMRI, meet NIHSS and exclude hemorrhagic stroke Lower Limb Thrombos:ultr
Index test:Biomarkers: Serum levels of P-selectin (CD62P),E-selectin (CD62E),Intercellular Adhesion Molecule-1 (ICAM-1
CD54),Vascular Cell Adhesion Molecule-1 (VCAM-1
CD106) Galectin-3 (Gal-3),Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1
CD31,von Willebrand Factor (VWF)

Sponsors

Shandong Provincial Qianfoshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Disease group: adult patients (>18 years old) diagnosed with myocardial infarction, cerebral infarction and lower extremity arteriovenous thrombosis, regardless of gender, and meeting the diagnostic criteria of the corresponding diseases (WHO/NINDS/imaging). 2. Inclusion criteria for the control group: age (>18 years), gender is not restricted

Exclusion criteria

Exclusion criteria: 1. Disease group exclusion criteria: (1) Autoimmune diseases (e.g., systemic lupus erythematosus, rheumatoid arthritis, antiphospholipid syndrome) may influence inflammatory responses and adhesion molecule expression. (2) Chronic infectious diseases (e.g., HIV, tuberculosis, chronic hepatitis) may alter adhesion molecule levels through immune activation. (3) Malignant tumours (particularly haematological malignancies or metastatic tumours) may be associated with systemic inflammation or coagulation abnormalities. (4) Severe hepatic or renal dysfunction (e.g., elevated serum creatinine, markedly abnormal transaminase levels) may affect sample metabolism or test accuracy. Concurrent benign colorectal conditions (e.g., ulcerative colitis, colorectal adenomas, polyps) or tumours other than colorectal carcinoma. 2. Exclusion criteria for the control group: tumours; any abnormal findings in complete blood count, urinalysis, blood biochemistry, urine biochemistry, liver/kidney function tests, or blood glucose.

Design outcomes

Primary

MeasureTime frame
Diagnosis;Diagnosis;Diagnosis;Diagnosis;Diagnosis;Diagnosis;

Secondary

MeasureTime frame
Diagnosis;

Countries

China

Contacts

Public ContactXiaohong Shi

Shandong Provincial Qianfoshan Hospital

s20739@163.com+86 531 89269681

Outcome results

None listed

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