Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05741905

Safety and Efficacy of Levofloxacin Combined With Intravenous Thrombolysis for Acute Ischemic Stroke

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Yi Yang · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the efficacy and safety of levofloxacin combined with intravenous thrombolysis in treating acute ischemic stroke

Detailed description

Acute ischemic stroke is a leading cause of disability and mortality. Intravenous thrombolysis is a major therapy for acute ischemic stroke, however, nearly half of patients failed to benefit from it. It is necessary to find new interventions combined to intravenous thrombolysis, which promote the efficacy of intravenous thrombolysis. The investigators' previous studies suggested levofloxacin to be a newly identified neuro-protective agent, which could reduce infarct volume and improve neurologic function in animal models. To evaluate the efficacy and safety of levofloxacin combined with intravenous thrombolysis in treating acute ischemic stroke patients, the prospective, multicenter and randomized controlled trial was designed.

Conditions

Interventions

TypeNameDescription
DRUGLevofloxacinLevofloxacin is a quinolone antibiotics and newly identified neuro-protective agent. Intravenous thrombolysis is one of the treatments for acute ischemic stroke.
DRUGLevofloxacin simulantLevofloxacin simulant is placebo. Intravenous thrombolysis is one of the treatments for acute ischemic stroke.

Timeline

Start date
2023-06-01
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2023-02-23
Last updated
2024-10-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05741905. Inclusion in this directory is not an endorsement.