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Study identifier: NCT06654453 Synced from ClinicalTrials.gov · July 29, 2026
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The Thrombus Aspiration During PCI After Thrombolysis in STEMI

Condition: ST-segment Elevation Myocardial Infarction  ·  Sponsor: Shenghua Zhou

PhaseNA
Planned participants3500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to determine whether thrombus aspiration combined with percutaneous coronary intervention (PCI) improves clinical outcomes in ST-segment elevation myocardial infarction (STEMI) patients with high thrombus burden post-thrombolysis, compared to PCI alone. The study population includes 3500 STEMI patients, confirmed by diagnosis, who are transferred to PCI centers after receiving thrombolysis and have no contraindications to thrombolysis.The main questions it aims to answer are: 1. Does thrombus aspiration reduce 30-day major adverse cardiovascular events (MACE), including cardiovascular death, recurrent myocardial infarction, stroke, or heart failure rehospitalization? 2. Can thrombus aspiration improve microcirculation and clinical outcomes for high thrombus burden patients after thrombolysis? Researchers will compare patients randomly assigned to receive thrombus aspiration combined with PCI versus those who receive PCI alone to evaluate the effects on reducing MACE and improving clinical recovery. Participants will: Undergo initial thrombolysis followed by transfer to PCI centers. Be randomly assigned in a 1:1 ratio to receive either thrombus aspiration combined with PCI or PCI alone. Be followed for 30 days post-treatment to assess MACE and other clinical outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Shenghua Zhou  ·  073185292012  ·  zhoushenghua@csu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Department of General Surgery, The Second Xiangya Hospital of Central South University, No. 139, Middle Renmin Road, Changsha, 410011 Hunan, PR ChinaChangsha, Hunan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06654453