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Diagnostic Accuracy of Serum Biomakers in the Super-acute Ischemic Stroke (BIOSIS)

The molecular classification diagnosis and treatment of super early ischemic stroke with blood biomakers / Screening for the blood biochemical markers of diagnosis and treatment of the classification of super early stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DPD-15006027
Enrollment
Unknown
Registered
2015-03-02
Start date
2015-03-10
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Super-acute Ischemic Stroke

Interventions

Gold Standard:
Index test:

Sponsors

Zhengzhou University People's Hospital or Henan Province People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Patients with time window between symptom onset and hospital admission from 0 to 12h, the onset time is the finally time of normal state (such as, when patients wake up, the stroke onset to think the time is just or again sleeping); 2) Presence of a hemiparesis at hospital admission (i.e., unilateral paresis of arm and leg), unilateral deep sensation obstacle, aphasia, neglect, homonymous hemianopia, gaze deviation to the contralateral side of the hemiparesis, reduced level of consciousness, etc.; 3) Adults, 18 to 80 years; 4) Having signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients are dignosed with acute ICH or cerebrovascular malformation; 2) Patients had an encephalitis or cephalomeningitis, a pneumonia, a gastroenteritis or a urinary tract infection within nearly three weeks; 3) Patients were excluded if they had a transient ischemic attack, an ischemic stroke, an ICH, a brain trauma, myocardial infarction, myocarditis and pericarditis within 3 months before the index event. 4) Patients had a brain surgery within 3 months; 5) Patients are suffering from some late nervous or mental illnesses such as dementia, Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis and schizophrenia, needed 1~2 people to help; 6) Patients had a diagnosis of primary or metastatic brain tumor at any time in their medical history; 7) Patients have a terminal stage disease, such as, left or right heart failure, liver failure, renal failure, and others in a state of cachexia, or dyscrasia; 8) Pregnants or lactating women; 9) Patients have some contraindications of MRI, such as claustrophobia, heart pacemakers, confusion, or metallic implants; 10) Patients are in other clinical researches.

Design outcomes

Primary

MeasureTime frame
UCHL1;

Secondary

MeasureTime frame
the size of lesion;NIHSS and GCS score;the classification about ASCO;

Countries

China

Contacts

Public ContactXiong Han
hanxiong7589@126.com+86 13837171615

Outcome results

None listed

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