← Eichor
Study identifier: NCT06955936 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efferon CT Hemoadsorption for Cardiogenic Shock in Acute Myocardial Infarction

Condition: Myocardial Infarction · Cardiogenic Shock  ·  Sponsor: Efferon JSC

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Cardiogenic shock is the most severe manifestation of acute heart failure and remains the leading cause of death in patients hospitalised with acute myocardial infarction. Cardiogenic shock is a well-known and potent trigger of the immune response, ischemia/reperfusion organ damage, hemolysis and release of free hemoglobin. The activation of immune cells leads to the release of cytokines and inflammatory mediators such as IL-6, IL-8, activated complement and others. As a result of myocardial ischaemia and reperfusion injury, a multiorgan dysfunction syndrome may develop. The Efferon CT hemoadsorption device effectively removes cytokines and other pro-inflammatory molecules (≤55 kDa). This study evaluates whether this blood-filtering therapy can prevent organ failure in acute myocardial infarction patients with cardiogenic shock by eliminating inflammation-inducing mediators.

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

Talk to the study team

Alexandr Shelehov-Kravchenko, PhD, MD  ·  +79636564765  ·  alexandr.shelehov@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tomsk NRMC Cardiology Research InstituteTomsk, RussiaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06955936