Skip to content

The study of clinical efficacy of platelet GPII b / III a receptor antagonist in the treatment of acute non-cardiac stroke which screened by imaging

The study of clinical efficacy of platelet GPII b / III a receptor antagonist in the treatment of acute non-cardiac stroke which screened by imaging

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046570
Enrollment
Unknown
Registered
2021-05-22
Start date
2021-05-10
Completion date
Unknown
Last updated
2022-01-04

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:intravenous infusion of tirofiban
control group:Standard antiplatelet therapy

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. Aged 18 to 80 years; 2. The onset time is 6-72h; 3. Symptoms fluctuate within 24 hours of onset; 4. Admission NIHSS score 4-10 points; 5. Brain MRI showed that the lesion on DWI was less than 1/3 of the area dominated by MCA/PCA or there were multiple spots, small patches or irregular high signals. MRA ruled out large vessel occlusion, and brain CT ruled out intracranial hemorrhage; 6. ECG and ECG monitoring to rule out heart diseases such as atrial fibrillation; 7. Having two or more of high-risk factors such as hypertension, hyperlipidemia, and hyperglycemia; 8. The family members sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with thrombolysis and thrombectomy; 2. Intracranial stenosis and occlusion of large blood vessels; 3. Past history of intracranial hemorrhage; 4. Platelet count 185mmHg or diastolic blood pressure>110mmHg; 7. Patients with severe liver and kidney insufficiency or severe diabetes; 8. Patients with incomplete information.

Design outcomes

Primary

MeasureTime frame
Symptomatic intracranial hemorrhage;NIHSS score;mRS score after three months treatment;Blood cell test;Blood coagulation index;Changes of infarct size in MRI;Non-symptomatic hemorrhage;

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 4, 2026