Clinical Trials Directory

Trials / Completed

CompletedNCT06018181

Outcomes After Intravenous Alteplase / Tenecteplase With or Without Shuxuetong Injection in Routine Clinical Practice

Outcomes After Intravenous Alteplase / Tenecteplase With or Without Shuxuetong Injection in Routine Clinical Practice: A Patient Registry

Status
Completed
Phase
Study type
Observational
Enrollment
2,408 (actual)
Sponsor
Dongzhimen Hospital, Beijing · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGShuxuetong InjectionAccording to clinical real treatment records

Timeline

Start date
2023-09-28
Primary completion
2025-08-28
Completion
2025-09-03
First posted
2023-08-30
Last updated
2026-02-27

Locations

78 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06018181. Inclusion in this directory is not an endorsement.