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

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Diagnosis of first acute STEMI in accordance with the European Society of Cardiology (ESC) Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation

• Symptoms consistent with STEMI with beginning greater than 30 minutes but less than 12 hours prior to primary percutaneous coronary intervention (PCI)

• CRP elevation of ≥7 mg/l measured between 6 to 16 hours after primary PCI

• Eligible for primary PCI

• Age ≥18 years

• Written informed consent

Locations
Other Locations
Austria
University Clinic for Cardiology and Nephrology, Medical University of Graz
RECRUITING
Graz
University Clinic of Internal Medicine III, Cardiology and Angiology. University Clinic of Internal Medicine IV, Nephrology and Hypertensiology. University Clinic of Radiology.
RECRUITING
Innsbruck
University Clinic of Internal Medicine II, Paracelsus Medical University Salzburg
NOT_YET_RECRUITING
Salzburg
Germany
Leipzig Heart Center
RECRUITING
Leipzig
Medical Clinic II - University Heart Center Lübeck
NOT_YET_RECRUITING
Lübeck
Contact Information
Primary
Sebastian J Reinstadler, MD, PhD
sebastian.reinstadler@gmail.com
+43 (0) 512 504 25665
Backup
Ivan Lechner, MD, PhD
ivan.lechner@tirol-kliniken.at
+43 (0) 512 504 25665
Time Frame
Start Date: 2021-04-01
Estimated Completion Date: 2025-08-31
Participants
Target number of participants: 202
Treatments
Experimental: Selective 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.
No_intervention: Standard of care according to current guideline recommendations
Related Therapeutic Areas
Sponsors
Leads: Medical University Innsbruck

This content was sourced from clinicaltrials.gov