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Clinical Trial Summary

Acute ischemic stroke is one of the main diseases leading to high risk of disability and morbidity worldwide. Since intravenous thrombolysis(IVT) can effectively improve the long-term functional prognosis of acute ischemic stroke(AIS), IVT within 4.5 hours of onset has been widely recommended by international guidelines. Although 35-53% of AIS patients achieve functional independence after receiving IVT, there are still a large number of patients who are disabled or even dead, and nearly 70% of patients have ineffective recanalization. Therefore, there is an urgent need for therapeutic drugs after IVT to further improve the prognosis and reduce the burden of AIS. Shuxuetong injection is widely used in China in patients with AIS after IVT, but the situation in real clinical practice is unclear. Therefore, the study aims to evaluate the effectiveness and safety of Shuxuetong Injection in patients with AIS treated with intravenous alteplase and tenecteplase, and obtain high-quality clinical evidence.


Clinical Trial Description

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Study Design


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NCT number NCT06018181
Study type Observational [Patient Registry]
Source Dongzhimen Hospital, Beijing
Contact Mingzhen Qin
Phone 86-17801222857
Email qinmz@bucm.edu.cn
Status Not yet recruiting
Phase
Start date September 1, 2023
Completion date December 31, 2025