Ireland
--:--IST
Recruiting Observational

Protective Effect of Early High Dose stATins On Cardiovascular and Renal Events in Acute Coronary Syndrome

NCT04087200 · tracked via the Priya Life Science Italy tracker
Sponsor
Centro Cardiopatici Toscani
Phase
Observational
Started
2016-12-01
Last updated
2019-09-12

Condition(s) studied

Acute Coronary Syndrome

Study summary

Registration of all ACS patients (STEMI and NSTEMI) admitted to the cardiology ward and scheduled for early invasive strategy. The aim is to evaluate the protective effects of early (on admission) high-dose high-potency statin therapy on early and mid-term cardiac and renal events in this subset of patients.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Acute coronary syndrome (ST elevation and non ST elevation) * Early invasive strategy Exclusion Criteria: * contraindication to statin therapy * refusal of consent

Primary outcome measure(s)

  • Acute renal function changes — Within 72 hours after hospital admission
    Changes in creatinine and/or cystatine values
  • Inflammatory profile changes — up to 1 month
    Changes from baseline in CRP values
  • Lipid profile changes — up to 1 month
    Changes from baseline in cholesterol values
  • Platelet count — up to 1 month
    Changes from baseline in platelet count
  • Platelet volume — up to 1 month
    Changes from baseline in platelet volume
  • Platelet aggregation profile — up to 1 month
    Changes from baseline in platelet reactivity (Verify Now)

Trial sites (1)

FacilityCityRegionStatus
Cardiology Division, Prato Hospital Prato Italy Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04087200 on ClinicalTrials.gov ↗ ← All trials in Italy