Pro-urokinase for Extended-Window Posterior Circulation Stroke

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital of Zhengzhou University

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

Treatment groups

586 Participants
are divided into 2 treatment groups