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the study of Clinical efficacy of low-dose rt-PA combined with tirofiban in the treatment of non-cardiac acute cerebral infarction

the study of Clinical efficacy of low-dose rt-PA combined with tirofiban in the treatment of non-cardiac acute cerebral infarction

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014666
Enrollment
Unknown
Registered
2018-01-28
Start date
2018-02-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

Cerebrovascular disease

Interventions

test group:Low-dose alteplase and tirofiban
Control group:standard single-dose rt-PA treatment

Sponsors

Department of Neurology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. age = 18 years; 2. onset 4.5h; 3. diagnosis of ischemic stroke, a clear neurological deficit; 4. no prior atrial fibrillation, severe heart disease patients; 5. admission NIHSS score <15 points; 6. brain CT has ruled out intracranial hemorrhage; 7. family members signed informed consent.

Exclusion criteria

Exclusion criteria: 1. More than 4.5h onset of patients; 2. Previous history of atrial fibrillation or severe heart disease; 3. Previous history of intracranial hemorrhage; 4. symptoms suggest subarachnoid hemorrhage; 5. existence of intracranial tumors, arteriovenous malformations or aneurysms; 6. nearly 3 months have a history of severe head injury or cerebral infarction, but does not include the old small lacunar infarction Symptoms and signs; 7. nearly a week difficult to oppress the site of hemostasis arterial puncture; 8. severe liver and kidney dysfunction or severe diabetes; 9. accompanied by active bleeding; 10. blood glucose 185 mmHg or diastolic blood pressure> 110 mmHg; 11. Platelet count below normal; oral anticoagulant with INR> 1.7.

Design outcomes

Primary

MeasureTime frame
NIHSS score;mRS score three months after thrombolysis;symptomatic hemorrhage;Non-symptomatic hemorrhage;Blood coagulation index;Blood cell test;

Countries

China

Contacts

Public ContactLiang Zhigang

Department of Neurology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University

zgliang@hotmail.com+86 13723987720

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026