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NOT YET RECRUITING
NCT07842185
PHASE2/PHASE3

A Multicenter, Three-Arm, Open-Label, Endpoint-Blinded Randomized Controlled Trial to Evaluate the Optimal Duration of Early Tirofiban After Intravenous Thrombolysis in Acute Ischemic Stroke

Sponsor: Xinqiao Hospital of Chongqing

View on ClinicalTrials.gov

Summary

Acute ischemic stroke is a leading cause of disability and mortality among dults in China. Although intravenous thrombolysis serves as first-line reperfusion therapy, nearly half of patients fail to achieve vascular recanalization. The reocclusion rate ranges from 14% to 34%, and many patients are left with residual neurological deficits. Early antiplatelet therapy initiated after thrombolysis may sustain persistent reperfusion and improve prognosis. However, current guidelines generally recommend delaying antiplatelet treatment until 24 hours post-thrombolysis due to bleeding risks, and direct evidence for the optimal initiation timing remains lacking. Tirofiban is a rapidly acting, short-half-life, reversible glycoprotein IIb/IIIa receptor antagonist. Previous studies indicate its potential benefits and acceptable safety when administered after intravenous thrombolysis. This is a multicenter, three-arm, open-label, endpoint-blinded randomized controlled trial. A total of 1482 non-cardioembolic patients without large or medium vessel occlusion and with residual neurological deficits (NIHSS ≥4) after thrombolysis will be enrolled. Participants will be randomly allocated to the tirofiban 24-hour group, tirofiban 48-hour group, or blank control group. The primary outcome is the proportion of patients with excellent functional outcome defined as modified Rankin Scale (mRS) score 0-1 at 90 days. Symptomatic intracranial hemorrhage and neurological outcomes will also be evaluated. The study aims to determine the optimal duration of tirofiban treatment after thrombolysis and provide high-level evidence for precise interventions in the acute phase of stroke.

Official title: A Multicenter, Three-Arm, Open-Label, Endpoint-Blinded Randomized Controlled Trial to Evaluate the Optimal Infusion Duration of Early Tirofiban Treatment After Intravenous Thrombolysis in Patients With Acute Ischemic Stroke (INSTANT-2)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

1482

Start Date

2026-11-19

Completion Date

2031-05-08

Last Updated

2026-09-25

Healthy Volunteers

No

Interventions

DRUG

Tirofiban Injection

Intravenous infusion of tirofiban will be initiated after intravenous thrombolysis and continued for 24 hours. The dosage regimen follows the trial protocol.

DRUG

Tirofiban Injection

Intravenous infusion of tirofiban will be initiated after intravenous thrombolysis and continued for 48 hours. The dosage regimen follows the trial protocol.

OTHER

No Interventions

No tirofiban will be administered after intravenous thrombolysis. Patients receive routine standard clinical management according to hospital guidelines.

Locations (10)

Taihe County People's Hospital

Fuyang, Anhui, China

Longyan First Hospital of Fujian Medical University

Longyan, Fujian, China

Xiangtan Central Hospital (The Affiliated Hospital of Hunan University)

Xiangtan, Hunan, China

Ganzhou People's Hospital

Ganzhou, Jiangxi, China

Xingguo People's Hospital, Xinguo Hospital of Gannan Medical University

Ganzhou, Jiangxi, China

Jingdezhen First People's Hospital

Jingdezhen, Jiangxi, China

The First People's Hospital of Jingdezhen City

Jingdezhen, Jiangxi, China

Jiujiang First People's Hospital

Jiujiang, Jiangxi, China

Dalian Central Hospital

Dalian, Liaoning, China

The First People's Hospital of Mianyang (Mianyang 404 Hospital)

Mianyang, Sichuan, China