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Safety and Efficacy of Intervention of Tirofiban during Perioperative period of Endovascular Therapy in Patients with Acute Ischemic Stroke

Safety and Efficacy of Intervention of Tirofiban during Perioperative period of Endovascular Therapy in Patients with Acute Ischemic Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ONN-17013511
Enrollment
Unknown
Registered
2017-11-23
Start date
2017-11-30
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

acute ischemic stroke

Interventions

tirofiban group:intravenous or intra-arterial tirofiban
Control:Mechanical thrombectomy and drug treatment programs include expansion, control of blood pressure, blood sugar, moderate sedation, etc.

Sponsors

Daping Hospital of Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. acute ischemic stroke patients with large artery occlusion detected by CTA or MRA, aged 18 years or older; 2. No evidence of Cardioembolism; 3. Patients presented to ER mores than 4.5 hours from symptom onset, the volume of infarct core less than volume of hypoperfusion area on CTP; 4. Patient or his/her relative was willing to participate in the study and to provide informed consent.

Exclusion criteria

Exclusion criteria: 1) Hemorrhagic transformation; 2) Pre-stroke mRS = 2; 3) History of severe bleeding or major surgery within 30 days; 4) Coexistent terminal illness with life expectancy = 12 months; 5) Any known hereditary or acquired hemorrhagic diathesis, coagulation factor deficiency; 6) taking oral anticoagulant with INR > 1.7; 7) Platelet count < 100,000/mm3; 8) Hemoglobin < 10 g/dL; 9) A serum glucose level= 50 mg/dl; or 10) Severe renal insufficiency with creatinine clearance rate <30ml/min; 11) patient or his/her relative refuses to use tirofiban.

Design outcomes

Primary

MeasureTime frame
hemorrhagic tranformaiton;mortality;NIHSS at 7 days;times of thrombectomy;time from puncture to TICI2b/3;

Secondary

MeasureTime frame
mRs at 90 days;

Countries

China

Contacts

Public ContactMeng Zhang

Neurology Department of Daping Hospital, Third Military Medical University

172228621@qq.com+86 023 68757816

Outcome results

None listed

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