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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorGeneral Hospital of Shenyang Military Region

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age: 18-80 years;

Patients with acute anterior circulation large vessel occlusion within 24 hours of onset who will receive endovascular treatment;

Pre-stroke mRS: 0-1;

Baseline NIHSS: ≥6;

Disqualifiers

The presence of contraindications to internal jugular vein cannulation;

Receiving intravenous thrombolysis;

Haemorrhagic stroke (cerebral haemorrhage or subarachnoid haemorrhage);

Coagulation disorders, systemic bleeding tendency, thrombocytopenia (<100×109/L);

Trial population

Patients with acute anterior circulation large vessel occlusion within 24 hours of onset who will receive endovascular treatment

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • endovascular treatment

    Procedure/Surgery

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

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Dynamic changes in serum biomarkers after endovascular treatment

These biomarkers will be identified based on proteomic methods

Time frame
from the baseline to immediately, 30 minutes, 6 hours, and 24 hours after endovascular treatment

Secondary outcomes

1

favourable functional outcome, defined as modified Rankin Scale (mRS) 0-2

mRS ranges from 0-6, high score means poor outcome

Time frame
90±7 days
2

excellent functional outcome, defined as modified Rankin Scale (mRS) 0-1

mRS ranges from 0-6, high score means poor outcome

Time frame
90±7 days
3

distribution of modified Rankin Scale (mRS) score

mRS ranges from 0-6, high score means poor outcome

Time frame
90±7 days
4

early neurological improvement, defined as 4 or more decrease in National Institute of Health stroke scale (NIHSS)

NIHSS ranges from 0-22, with high score meaning severe neurological deficit.

Time frame
24±8 hours

Other outcomes

1

the association between cerebral circulation time (CCT) and clinical outcomes

CCT is defined as the time from the appearance of contrast at the siphon segment of the internal carotid to the end of the arterial phase during DSA on the anteroposterior and lateral image in anterior circulation LVO; clinical outcomes include changes in NIHSS and mRS

Time frame
24±8 hours, 10±2 days, 90±7 days
2

the association between serum biomarkers and clinical outcomes

serum biomarkers include those in different timepoints or their dynamic changes; clinical outcomes include changes in NIHSS and mRS

Time frame
24±8 hours, 10±2 days, 90±7 days
3

the association between serum biomarkers and status of vessel recanalization

serum biomarkers include those in different timepoints or their dynamic changes; the status of vessel recanalization is determined by modified thrombolysis in cerebral infarction

Time frame
24±8 hours, 10±2 days, 90±7 days

Sponsors and contacts

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