Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04939805

CRP Apheresis in STEMI

Selective C-reactive Protein Apheresis in ST-elevation Myocardial Infarction

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
202 (estimated)
Sponsor
Medical University Innsbruck · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Background: In patients with acute ST-elevation myocardial infarction (STEMI), the amount of infarcted myocardium (infarct size) is known to be a major predictor for adverse remodeling and recurrent adverse cardiovascular events. Effective cardio-protective strategies with the aim of reducing infarct size are therefore of great interest. Local and systemic inflammation influences the fate of ischemic myocardium and thus, adverse remodeling and clinical outcome. C-reactive protein (CRP) also acts as a potential mechanistic mediator that adversely affects the amount of irreversible myocardial tissue damage after acute myocardial infarction. Objective: The main objectives of the current study are to investigate the efficacy of selective CRP apheresis, using the PentraSorb®-CRP system, as an adjunctive therapy to standard of care for patients with acute STEMI treated with primary PCI. Design: Investigator-initiated, prospective, randomized, open-label (outcome assessors masked), controlled, multicenter, two group trial with a two-stage adaptive design. Innovation: Selective CRP apheresis offers potential to decrease infarct size and consequently improve outcome after PCI for STEMI. This is the first randomized trial investigating the impact of selective CRP apheresis on infarct size in post-STEMI patients. In perspective, the study design allows furthermore to collect robust evidence for the design of a definitive outcome study.

Conditions

Interventions

TypeNameDescription
DEVICESelective CRP apheresis using the PentraSorb®-CRP systemSelective CRP apheresis as an adjunct to standard of care. Apheresis using the PentraSorb®-CRP system will be performed at day 1, 2 and 3 after PCI.

Timeline

Start date
2021-04-01
Primary completion
2025-08-31
Completion
2025-08-31
First posted
2021-06-25
Last updated
2025-05-09

Locations

5 sites across 2 countries: Austria, Germany

Source: ClinicalTrials.gov record NCT04939805. Inclusion in this directory is not an endorsement.