Clinical Trials in Italy / NCT04087200
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
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Cardiology Division, Prato Hospital | Prato | Italy | Recruiting |
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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