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NCT04087200: PRATO-ACS

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

Recruiting now Last updated 12 September 2019
What this trial tests

trial in Acute Coronary Syndrome in 2,500 participants. Currently enrolling.

Timeline
1 December 2016
Primary endpoint
1 December 2025
1 December 2026

Quick facts

Lead sponsorCentro Cardiopatici Toscani
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment2,500
Start date1 December 2016
Primary completion1 December 2025
Estimated completion1 December 2026
Sites1 location across Italy

Conditions studied

Sponsor

Centro Cardiopatici Toscani

Who can join

Eligibility, any sex, with Acute Coronary Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Biomarkers of residual risk and all-cause mortality after acute coronary syndrome.
    Toso A, Leoncini M, Maioli M, Villani S, et al · · 2025 · cited 5× · PMID 39896052 · DOI 10.1016/j.ajpc.2025.100934

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Other recruiting trials for Acute Coronary Syndrome

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04087200.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing