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Safety and efficacy of bridging arterial thrombolysis after successful recanalization in acute large vessel occlusion stroke

Safety and efficacy of bridging arterial thrombolysis after successful recanalization in acute large vessel occlusion stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300076881
Enrollment
Unknown
Registered
2023-10-23
Start date
2023-10-30
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

Stroke

Interventions

arterial thrombolysis group:NA

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1) age =18 years old; 2) the time from onset to treatment was within 24 hours; 3) anterior or posterior circulation large vessel occlusive stroke confirmed by CTA/MRA and the vessel responsible for signs and symptoms of acute ischemic stroke; 4) Alberta Stroke Program Early Diagnosis (ASPECTS) score of NCCT =6; 5) eTICI at least 2b after endovascular treatment; 6) Patients or their family members provided written informed consent.

Exclusion criteria

Exclusion criteria: 1) Intracranial hemorrhage confirmed by computed tomography (CT) or magnetic resonance imaging (MRI); 2) receiving intravenous thrombolytic therapy; 3) mRS Score =2 before onset; 4) Intraoperative DSA showed vascular perforation, dissection, and contrast extravasation; 5) pregnant or lactating women; 6) allergy to contrast media; 7) participating in other clinical research; 8) systolic blood pressure > 185mmHg or diastolic blood pressure > 110mmHg, and could not be controlled by oral antihypertensive drugs; 9) genetic or acquired bleeding constitution, anticoagulant factor deficiency; Or have oral anticoagulants and INR > 1.7; 10) Blood glucose 22.2mmol/L (400mg/dl), platelet 220µmol/L (2.5mg/dl)); 13) life expectancy due to advanced stage of any disease 3.

Design outcomes

Primary

MeasureTime frame
The rate of 90-day modified RANKIN scale (mRS) score 0-1 (%);mortality at 90 days;Incidence of symptomatic intracranial hemorrhage within 48 hours;

Secondary

MeasureTime frame
Shift in the distribution of mRS scores at 90 days;Proportion of patients with functional independence (mRS score 0 to 2) at 90 days;

Countries

China

Contacts

Public ContactYangmei Chen

The Second Affiliated Hospital of Chongqing Medical University

chenym1997@sina.com+86 136 0834 8562

Outcome results

None listed

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