About this trial
This study aims to evaluate whether, in patients with imaging-confirmed acute ischemic stroke of the posterior circulation presenting within 4.5-24 hours after symptom onset and not scheduled for endovascular thrombectomy, intravenous thrombolysis with recombinant human prourokinase (rhPro-UK), compared with standard medical treatment, can achieve superior 90-day functional outcomes with a higher level of safety.
Eligibility criteria
Qualifiers
Age ≥ 18 years;
AIS with symptom onset 4.5-9 hours before enrollment, including wake-up stroke and unwitnessed stroke (onset time defined as when symptoms were first noticed);
DWI-FLAIR mismatch: visible lesion on DWI with no marked visible lesion on FLAIR;
DWI infarct core not exceeding one-third of the middle cerebral artery territory, one-half of the anterior cerebral artery territory, or one-half of the posterior cerebral artery territory;
Disqualifiers
Planned endovascular treatment;
Contradictory to MRI examination;
MRI image not qualified for evaluation;
Serious neurological deficits before onset (mRS≥2);
Trial design
Treatments tested in this trial
- rhPro-UK
- placebo
- Aspirin
- Placebo