Treatment of ACuTe Coronary Syndromes With Low-dose colchICine

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBeijing Anzhen Hospital

About this trial

This trial is designed to evaluate whether low-dose colchicine, in addition to standard treatment recommended by guidelines, further reduces the risk of major adverse cardiovascular events in patients with acute coronary syndromes (ACS) through a prospective, randomized, double-blind, placebo-controlled clinical trial.

Eligibility criteria

Qualifiers

Age ≥ 18 years;

Definite diagnosis of ACS;

Ability and willingness to provide written informed consent

Disqualifiers

Type 2 myocardial infarction (Patients with symptoms or signs of myocardial ischemia and evidence of increased oxygen demand or decreased supply [for example, tachyarrhythmia, hypotension, or anaemia] secondary to an alternative pathology and myocardial necrosis are defined as suffering type 2 myocardial infarction. The classification of type 2 myocardial infarction also includes patients with coronary vasospasm, embolism or spontaneous dissection without evidence of atherothrombosis related to coronary artery disease);

Valvular heart disease that is considered likely to require surgical intervention;

History of non-skin cancer in the past 3 years;

Inflammatory bowel disease or chronic diarrhea;

Trial design

Treatments tested in this trial

  • Colchicine Pill
  • Placebo

Treatment groups

6,574 Participants
are divided into 2 treatment groups

Sponsors and collaborators