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Search / Trial NCT05250596

COLchicine On-admission to Reduce Inflammation in Acute Coronary Syndrome (COLOR-ACS)

Launched by AZIENDA USL TOSCANA CENTRO · Feb 20, 2022

Trial Information

Current as of June 08, 2025

Completed

Keywords

Colchicine Atorvastatin Acute Coronary Syndrome C Reactive Protein Acute Kidney Injury

ClinConnect Summary

On-admission all statin naive NSTEACS patients are randomized to receive either standard treatment of atorvastatin 80 mg or standard treatment plus colchicine (1 mg loading dose followed by 0.5 mg/day).

Inflammatory biomarker high sensitivity C reactive protein (hs-CRP) is measured in all patients on-admission and every 24 hours thereafter until discharge.

Cardiac and renal function parameters are evaluated to evidence the possible beneficial effects of the administration of colchicine in addition to atorvastatin alone both short- and medium-term (up to 30 days).

Colchicine tolerance is ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • non-ST elevation acute coronary syndrome;
  • ≥ 18 years;
  • statin-naive.
  • Exclusion Criteria:
  • prior statin therapy and/or colchicine treatment;
  • known allergy or hypersensitivity to colchicine or statins;
  • current treatment with potent inhibitors of CYP3A4 or P-glycoprotein (eg., Cyclosporin, antiretroviral drugs, antimycotics, erythromicin and clarythromycin);
  • previous or scheduled administration of any immunosuppressive therapy;
  • known active malignancy;
  • severe kidney disease (creatinine \> 3 mg/dl or dialysis)
  • severe liver disease (ALT and/or AST, \> double ref. normal values in case of (a) total bilirubin \> double ref. normal values, or (b) alteration in coagulation (INR\> 1,5);
  • severe heart failure (NYHA class ≥ 3 or cardiogenic shock) at hospital presentation;
  • severe acute or chronic gastro-intestinal disease (nausea, vomiting, diarrhea, malabsorption disease, malnutrition);
  • pregnancy or lactation;
  • current COVID-19 or other infectious disease;
  • refusal of consent.

About Azienda Usl Toscana Centro

Azienda USL Toscana Centro is a prominent healthcare organization based in Tuscany, Italy, dedicated to delivering high-quality medical services and advancing public health through innovative research. As a clinical trial sponsor, it plays a crucial role in the design, execution, and management of clinical studies aimed at evaluating new therapies and improving patient outcomes. The organization emphasizes collaboration with academic institutions, industry partners, and regulatory bodies to ensure rigorous adherence to ethical standards and scientific integrity. Committed to enhancing healthcare delivery, Azienda USL Toscana Centro strives to translate research findings into tangible benefits for the community it serves.

Locations

Pescia, , Italy

Pistoia, , Italy

Prato, , Italy

Patients applied

0 patients applied

Trial Officials

Anna Toso, MD

Principal Investigator

Santo Stefano Hospital, Prato, Italy

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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