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Clinical application of multimodal evaluation and individualized treatment in patients with acute cerebral infarction after ineffective intravenous thrombolysis or arterial thrombectomy

Clinical application of multimodal evaluation and individualized treatment in patients with acute cerebral infarction after ineffective intravenous thrombolysis or arterial thrombectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058513
Enrollment
Unknown
Registered
2022-04-10
Start date
2022-04-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

stroke

Interventions

intervention group:Tirofiban was used after intravenous thrombolysis
control group:Routine treatment after intravenous thrombolysis

Sponsors

Kunshan First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for acute ischemic stroke; 2. Acute stroke patients with hyperactivity and intravenous thrombolysis time window (contraindications refer to the Scientific Statement of the Chinese Stroke Society for Intravenous Thrombolysis of Acute Ischemic Stroke and the Chinese Guidelines for Early Endovascular Intervention for Acute Ischemic Stroke 2018); 3. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Accompanied by seizures; 2. Present or past 6 months of significant hemorrhagic disease; 3. History of severe central nervous system damage (e.g. tumor, aneurysm, arteriovenous malformation, intracranial or spinal cord surgery); 4. Patients with mental disorders, including schizophrenia or other mental illnesses; 5. Patients with severe liver and kidney insufficiency; 6. Patients who are allergic to tirofiban hydrochloride and have thrombocytopenia or agattriban after previous use of tirofiban hydrochloride are not suitable for anti-platelet aggregation.

Design outcomes

Primary

MeasureTime frame
Aggravation of neurological symptoms;

Secondary

MeasureTime frame
Intracerebral hemorrhage transformation;

Countries

China

Contacts

Public ContactZhang Yan

Kunshan First People's Hospital

1169364487@qq.com+86 13962638897

Outcome results

None listed

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