ST-segment Elevation Myocardial Infarction

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Review clinical trials related to ST-segment Elevation Myocardial Infarction. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Ischemic Postconditioning in STEMI Patients Treated With Primary PCI

In a prospective, randomized clinical trial the iPOST2 trial will determine whether ischemic postconditioning reduces reperfusion injury and this will translate into improved clinical outcome of heart failure and death for STEMI patients who present with TIMI0-1 undergoing primary PCI

Participants needed: 1,800
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Rigshospitalet, DenmarkUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Age ≥18 years [+3]

Potential pregnancy [+3]

Status: Recruiting

The Thrombus Aspiration During PCI After Thrombolysis in STEMI

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.

Participants needed: 3,500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shenghua ZhouUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Diagnosed with STEMI. [+3]

Contraindications for thrombolysis. [+5]

Status: Not yet recruiting

The FAVOR V AMI Trial

The FAVOR V AMI study is a prospective, multicenter, blinded, randomized, sham-controlled trial comparing the long-term clinical outcomes of the "Functional and Angiography-derived Strain inTegration (FAST)" technique (next-generation quantitative flow ratio \[μQFR\] and radial wall strain \[RWS\]) guided percutaneous coronary intervention (PCI) strategy, with standard treatment strategy, in patients with ST-segment elevation myocardial infarction (STEMI) and multivessel coronary disease (MVD).

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: China National Center for Cardiovascular DiseasesUpdated: Sep 13, 2023
Eligibility criteria

General inclusion [+7]

General exclusion [+15]