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The safety and efficacy of tirofiban prior to stenting for intracranial atherosclerotic stenosis

The safety and efficacy of tirofiban prior to stenting for intracranial atherosclerotic stenosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031935
Enrollment
Unknown
Registered
2020-04-15
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

intracranial atherosclerotic disease

Interventions

tirofiban group:give tirofiban
non-tirofiban group:not give tirofiban

Sponsors

The First Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. aged 50-80 yeas, male or female; 2. mRS <= 2; 3. symptomatic intracranial atherosclerotic disease (TIA or stroke) within 90 days; 4. the lesion was certified by DSA, incluing MCA-M1,BA,the intracranial segment of ICA or VA; 5. the stenosis degree was 70%-99% determined by WASID; 6. the etiological type is large artery atherosclerotic; 7. with written consent.

Exclusion criteria

Exclusion criteria: 1. aucte ischemic stroke within 1 week; 2. perforator stroke; 3. with tandem lesions; 4. anatomic tortuosity, the stent might not be placed; 5. non-atherosclerotic stenosis: such as dissection, moyamoya, et al; 6. cardiogenic stroke; 7. with tumor, aneurysm; 8. with the history of stenting in ex- or intracranial artery; 9. with the history of intracranial hemorrhage; 10. with thrombosisi within 24 hours befor group; 11. with neurological deterioration withn 24 hours; 12. with SAH within 30 days; 13. with myocardial infarction within 30 days; 14. with operation within 30 days; 15. be allergic to the drugs or devices; 16. ejection fraction <= 40%; 17. HB <= 100g/L, PLT <= 100*10^9/L; 18. severe dysfunction of liver or kidney; 19. active peptic ulcer; 20. life expectancy < 12 months; 21. can not complete the follow-up; 22. on other clinical trials.

Design outcomes

Primary

MeasureTime frame
the incidence of in-stent thrombosis;periprocedural new-onset stroke events;the incidence of symptomatic intracranial hemorrhage during periporcedure;

Secondary

MeasureTime frame
the DWI abnormity of periprocedural;the incidence of in-stent restenosis at 6 months;the ischemic events within 30 days;the residual stenosis after stenting;the incidence of asymptomatic intracranial hemorrhage during periprocedure;the incidence of bleeding other than the intracranial;the reduction of platelet;

Countries

China

Contacts

Public ContactJu Han

The First Affiliated Hospital of Shandong First Medical University

hanjujack@163.com+86 13791120710

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026