Condition: Stroke · Sponsor: Beijing Tiantan Hospital
The benefit-risk profile of thrombolysis for acute ischemic strokes beyond 24 hours has never been investigated. We initiated a multicenter, prospective, randomized, open label, blinded-endpoint (PROBE) controlled trial to assess the safety and efficacy of tenecteplase (0.25mg/kg, max 25mg) versus standard medical treatment in acute ischemic stroke due to intracranial vessel occlusion between 24-72 hours of symptom onset (including wake-up stroke and unwitnessed stroke).
This description comes directly from the study's public registry record.
Yongjun Wang · 86-10-59978350 · yongjunwang@ncrcnd.org.cn
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| Beijing tiantan hospital | Beijing, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06954155