Non-immunogenic Staphylokinase in Reperfusion Therapy of Ischemic Stroke in Routine Clinical Practice

ConditionAcute Stroke
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorNational Society for Neurosonology and Cerebral Circulation

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 volunteers

Qualifiers

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

Design model

Case-only

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Proportion of intracerebral hemorrhage

Number and proportion of intracerebral bleeding of any type, which occurs as a complication of thrombolytic treatment

Time frame
36 hours

Secondary outcomes

Other outcomes

Sponsors and contacts

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