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Change in Serum Biomarkers After Endovascular Treatment for Acute Anterior Circulation Large Vessel Occlusion

Change in Serum Biomarkers After Endovascular Treatment for Acute Anterior Circulation Large Vessel Occlusion: a Prospective, Registry Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06383182
Enrollment
800
Registered
2024-04-25
Start date
2024-07-02
Completion date
2027-12-30
Last updated
2026-09-17

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

Conditions

Ischemic Stroke

Brief summary

Acute ischaemic stroke (AIS) results in high rates of neurological morbidity and mortality, especially in patients with large vessel occlusion (LVO). Endovascular therapy (EVT) has been approved as the most effective treatment for patients with LVO , but about half patients undergoing EVT did not achieve good outcome. The mechanisms of poor prognosis are complex. How to accurately identify serological biomarkers related to patients' clinical prognosis is an important research topic nowadays.

Interventions

PROCEDUREendovascular treatment

all patients with anterior circulation large vessel occlusion will receive endovascular treatment.

Sponsors

General Hospital of Shenyang Military Region
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

1. Age: 18-80 years; 2. Patients with acute anterior circulation large vessel occlusion within 24 hours of onset who will receive endovascular treatment; 3. Pre-stroke mRS: 0-1; 4. Baseline NIHSS: ≥6; 5. Signed informed consent.

Exclusion criteria

1. The presence of contraindications to internal jugular vein cannulation; 2. Receiving intravenous thrombolysis; 3. Haemorrhagic stroke (cerebral haemorrhage or subarachnoid haemorrhage); 4. Coagulation disorders, systemic bleeding tendency, thrombocytopenia (\<100×109/L); 5. Severe cardiac, hepatic or renal insufficiency (ALT or AST elevated more than 2 times the upper limit of normal value, or serum creatinine elevated more than 1.5 times the upper limit of normal value or in need of dialysis) or other serious medical diseases; 6. Severe uncontrolled hypertension (systolic blood pressure greater than 200 mmHg or diastolic blood pressure greater than 110 mmHg); 7. Pregnant or lactating women; 8. Other conditions who are not suitable for this trial by investigator.

Design outcomes

Primary

MeasureTime frameDescription
Dynamic changes in serum biomarkers after endovascular treatmentfrom the baseline to immediately, 30 minutes, 6 hours, and 24 hours after endovascular treatmentThese biomarkers will be identified based on proteomic methods

Secondary

MeasureTime frameDescription
favourable functional outcome, defined as modified Rankin Scale (mRS) 0-290±7 daysmRS ranges from 0-6, high score means poor outcome
excellent functional outcome, defined as modified Rankin Scale (mRS) 0-190±7 daysmRS ranges from 0-6, high score means poor outcome
distribution of modified Rankin Scale (mRS) score90±7 daysmRS ranges from 0-6, high score means poor outcome
early neurological improvement, defined as 4 or more decrease in National Institute of Health stroke scale (NIHSS)24±8 hoursNIHSS ranges from 0-22, with high score meaning severe neurological deficit.
changes in National Institute of Health stroke scale (NIHSS)24±8 hoursNIHSS ranges from 0-22, with high score meaning severe neurological deficit.
symptomatic intracranial hemorrhage (sICH)24±8 hourssICH is defined as an increase in 4 or more points on the NIHSS
occurence of new stroke or other vascular events90±7 days

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026