About this trial
The study will collect data from aged 18 to 85 years with a diagnosis of acute stroke, who received thrombolytic treatment with a new agent, nonimmunogenic staphylokinase. Outcomes will be checked for safety and compared to the results of treatment with the other thrombolytic drug, alteplase.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 18-85 ;
Diagnosis of acute ischemic stroke eligible for thrombolytic therapy;
Thrombolytic therapy with the drug "non-immunogenic staphylokinase" is planned or has already been performed.
Disqualifiers
Individual intolerance or known hypersensitivity to a recombinant protein containing the amino acid sequence of staphylokinase;
The presence of a contraindication to thrombolytic therapy of ischemic stroke;
Pregnancy or lactation.
Trial population
Men and women aged 18 to 85 years (inclusive), who meet the inclusion criteria and do not have contraindications for thrombolysis, with a diagnosis of acute ischemic stroke.
Trial design
Case-only
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Proportion of intracerebral hemorrhage
Number and proportion of intracerebral bleeding of any type, which occurs as a complication of thrombolytic treatment
Sponsors and contacts
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