Skip to content

Efficacy and safety of tirofiban in bridging treatment of acute intracranial atherosclerotic vascular occlusion: a randomized controlled trial

Efficacy and safety of tirofiban in bridging treatment of acute intracranial atherosclerotic vascular occlusion: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022321
Enrollment
Unknown
Registered
2019-04-04
Start date
2019-04-15
Completion date
Unknown
Last updated
2019-04-08

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

Conditions

acute intracranial atherosclerotic vascular occlusion

Interventions

Treatment group:tirofiban hydrochloride injection

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age = 18 years; 2) the (mRS) score of modified Rankin scale before stroke was 0 or 1; 3) Intracranial hemorrhage, subarachnoid hemorrhage and space occupying were excluded by cranial CT; 4) intravenous thrombolysis with recombinant tissue plasminogen activator (rt-PA) within 4.5 hours and mechanical thrombectomy (through inguinal puncture) within 6 hours after onset, and intracranial atherosclerotic macrovascular occlusion was confirmed during the operation. 5) the subject (or the legal representative of the subject) signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1) there was a tendency of severe bleeding, intracranial hemorrhage or extracranial hemorrhage and active digestive tract ulcer in the past three months; 2) platelet count <100 × 10^9 /L; 3) hematological diseases; 4) patients with malignant tumor or other critically ill diseases; 5) cranial CT showed early and definite large area cerebral infarction of anterior circulation; 6) hypersensitivity to contrast medium; 7) lactating or pregnant women; 8) malignant hypertension without good control; 9) the degree of vascular distortion, variation and stenosis is serious and can not be operated; 10) end-stage disease, expected survival < 90 days, or expected inability to complete follow-up; 11) patients with severe injury and surgical history within 3 months; 12) those who are allergic to the study of drugs or drugs with similar chemical structures; 13) participated in other clinical trials or clinical study participants within 3 months prior to the start of this study; 14) the researchers do not consider it appropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Incidence of vascular re-occlusion;

Secondary

MeasureTime frame
90-day functional prognosis;Incidence of deterioration of neurological function within 24 hours;

Countries

China

Contacts

Public ContactDezhi Liu

Department of Neurology, Shanghai General Hospital

yzldz@126.com+86 13952002450

Outcome results

None listed

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