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Investigation on the workflow of intrahospital reperfusion therapy for acute ischemic stroke in county-level hospitals

Establishment and practice of an optimized intrahospital reperfusion therapy for acute ischemic stroke in secondary hospitals

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108454
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Acute ischemic stroke

Interventions

Intravenous thrombolysis:None

Sponsors

The Second Hospital & Clinical Medical School, Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, 2. Presenting with acute stroke with the clinical symptoms and signs, 3. Acute ischemic stroke was determined according to imaging examination (CT/MRI), 4. Patients who have indications for intravenous thrombolysis within 24 hours of onset according to guidelines, 4. Obtainment of informed consent from the patient or their legal guardian.

Exclusion criteria

Exclusion criteria: 1. Intracranial hemorrhage confirmed by cranial computed tomography (CT) or magnetic resonance imaging (MRI), including cerebral parenchymal hemorrhage, intraventricular hemorrhage, subarachnoid hemorrhage, subdural/extradural hematoma, etc; 2. History of prior intracranial hemorrhage; 3. Severe head trauma or stroke within the past 3 months; 4. Intracranial tumor, giant intracranial aneurysm; 5. Intracranial or intraspinal surgery within 3 months; 6. Major surgical procedures within the past 2 weeks; 7. Gastrointestinal or genitourinary bleeding within the past 3 weeks; 8. Active visceral bleeding; 9. Aortic arch dissection; 10. Arterial puncture at a non-compressible site within the previous week; 11. Elevated blood pressure: systolic pressure >180 mmHg or diastolic pressure >100 mmHg, and difficult to control with medication; 12. Acute bleeding tendency, including platelet count 1.7 or PT >15 s; 15. Use of thrombin inhibitors or Xa factor inhibitors within 48 hours, or abnormal laboratory tests (such as APTT, INR, platelet count, ECT, TT, or Xa factor activity assay, etc.); 16. Blood glucose level 22.22 mmol/L, and difficult to correct; 17.Head CT or MRI indicates a large area of infarction (infarction area>1/3 of the middle cerebral artery supply area); 18. Pregnancy or postpartum status; 19. In-hospital stroke; 20. Diagnostic workup is uncertain or suggests an event other than stroke as the likely cause.

Design outcomes

Primary

MeasureTime frame
door to needletime (DNT);Incidence of Symptomatic Intracranial Hemorrhage within 7 Days and 90-Day Mortality Rate;

Secondary

MeasureTime frame
Proportion of Cases with DNT <=60 Minutes (%);door to needletime, DNT;MRS (Modified Rankin Scale) score at 90 days;Incidence of asymptomatic intracranial hemorrhage (aSICH) within 7 days;Incidence of non-intracranial hemorrhagic complications (including gastrointestinal bleeding, urinary tract bleeding, oral or nasal mucosal bleeding, subcutaneous hematoma, etc.);Incidence of non-hemorrhagic serious adverse events (including cerebral herniation, pneumonia, respiratory failure, circulatory failure, stress ulcer, secondary epilepsy, urinary tract infection, sepsis, renal failure, acute coronary syndrome, venous thrombosis, and psychiatric symptoms, etc.);

Countries

China

Contacts

Public ContactZhang Zhenchang

The Second Hospital & Clinical Medical School, Lanzhou University

13893647595@163.com+86 138 9364 7595

Outcome results

None listed

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