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This study aims to evaluate whether initiating intravenous tirofiban within 48 hours of onset (with a 48-hour infusion), followed by sequential DAPT, can improve the likelihood of excellent functional...
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Lead Sponsor
Second Affiliated Hospital of Soochow University
Suzhou Municipal Hospital of Anhui Province
Suzhou, Anhui
Second Hospital of Hebei Medical University
Shijiazhuang, Hebei
Taikang Xian People's Hospital
Zhoukou, Henan
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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