Intravenous Adjuvant With Tirofiban Versus Alteplase Before Mechanical Thrombectomy in Acute Ischemic Stroke Patients With Large Vessel Occlusion: a Multicenter, Open Label, Randomized Controlled Trial.

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

In patients with acute ischemic stroke secondary to large vessel occlusion, the role of intravenous adjunctive medications, such as tirofiban, or alteplase before endovascular thrombectomy has not been well investigated. This trial aim to evaluate the efficacy and safety of intravenous tirofiban versus alteplase for acute ischemic stroke patients with large vessel occlusion piror to endovascular thrombectomy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged 18 years or older.

• Presenting with acute ischemic stroke symptom.

• Time from onset to hospital arrival:

‣ (1) within 4.5 hours

⁃ (2) 4.5-9.0 hours, image inclusion criteria for the EXTEND trial must be met

⁃ (3) \> 4.5 hours but within 24 hours, image inclusion criteria for the WAKE-UP trial must be met.

• Eligible for intravenous thrombolysis.

• Occlusion of the internal carotid artery, M1 or M2 segment of the middle cerebral artery, vertebrobasilar artery confirmed by CTA, MRA, or DSA.

• Informed consent obtained from patients or their legal representatives.

Locations
Other Locations
China
Hangzhou First People's Hospital
RECRUITING
Hangzhou
Contact Information
Primary
Hongfei Sang, Doctor
sanghongfei1988@163.com
+8613738132047
Backup
Zhongming Qiu, Doctor
qiuzhongmingdoctor@163.com
+8613236599269
Time Frame
Start Date: 2023-11-28
Estimated Completion Date: 2027-06-01
Participants
Target number of participants: 800
Treatments
Experimental: Tirofiban
Tirofiban will be administrated intravenously before endovascular thrombectomy.
Active_comparator: Alteplase
Alteplase will be administrated intravenously before endovascular thrombectomy.
Related Therapeutic Areas
Sponsors
Leads: Xinqiao Hospital of Chongqing
Collaborators: Zhejiang University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials