STEMI Treatment Optimization by Ischemic Postconditioning and IVUS Guidance
Recruiting now · Not applicable
Conditions studied: ST Elevation Myocardial Infarction
In brief
The purpose of is study is to investigate whether ischemic postconditioning (iPOST) and intravascular ultrasound-guided (IVUS) percutaneous coronary intervention (PCI) improve the clinical outcome of patients with ST-segment elevation myocardial infarction treated with primary PCI.
Key facts
- Study ID
- NCT04775914
- Run by
- Thomas Engstrom
- People needed
- 2500
- Starts
- 2021-04-01
- Expected to finish
- 2031-02-01
- Last updated by the study team
- 2026-03-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥18 years
- Acute onset of chest pain with <12 hours duration
- STEMI as characterized by 2 mm ST elevation in 2 or more V1 through V4 leads or presumed new left bundle branch block with minimum of 1 mm concordant ST elevation or 1 mV ST-segment elevation in the limb lead (II, III and aVF, I, aVL) and V4-V6 or ST depression in 2 or more V1 through V4 leads indicating posterior AMI.
- Exclusion Criteria (iPOST2):
- Pre-PCI TIMI flow 0 or 1 Potential pregnancy Inability to provide informed consent Unwillingness to consent Unavoidable to use thrombectomy Spontaneous coronary artery dissection Time from symptoms onset to PPCI > 12 hours Culprit in bypass graft Other reason for not including the patient
- Exclusion Criteria (iSTEMI):
- Potential pregnancy Inability to understand information in order to provide informed consent Unwillingness to consent Spontaneous coronary artery dissection Time from symptoms inset to PPCI > 12 hours Culprit in bypass graft Other reason
Where it is running
- Heart Center, Rigshospitalet — Copenhagen, Capital Region, Denmark (enrolling)
Full record on ClinicalTrials.gov
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