Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT04939805 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

CRP Apheresis in STEMI

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Primary completion date changed from estimate of Aug 31, 2025 to Jan 28, 2026
    • Study completion pushed from Aug 31, 2025 to Dec 15, 2026
    • Eligibility criteria expanded, about 18 words
    • Publications: details revised at 1 of 1 entry
  2. Notable Primary completion date: Mar 31, 2024 to Aug 31, 2025
    • Study completion date: Mar 31, 2025 to Aug 31, 2025
    v4
  3. Minor Site details revised at 2 of 5 sitesv3
  4. Minor Enrollment target: 170 to 202
    • Study sites: 4 to 5
    • Secondary endpoints: 15 to 16
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT04939805
Lead Sponsor Medical University Innsbruck
Conditions
(from sponsor)
ST Elevation Myocardial Infarction, C-Reactive Protein, Apheresis, Myocardial Injury
Related terms ST Elevation Myocardial Infarction
Enrollment 202 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov