Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:24 PM
Ignite Modification Date:
2025-12-24 @ 7:24 PM
NCT ID:
NCT02162303
Eligibility Criteria:
Inclusion Criteria:
* Male and female patients providing informed consent
* Patient must have evidence of coronary artery disease (CAD) as evidenced by at least one of the following:
* Angiographic evidence of at least 50% stenosis in one coronary artery (except for left main coronary artery stenosis, in which 30% is acceptable)
* History of prior percutaneous coronary intervention (PCI)
* History of prior acute coronary syndrome (ACS) event (ST elevation myocardial infarction (STEMI), non-STEMI or unstable angina)
* Patient has a carotid or ascending aorta atherosclerotic plaque inflammation TBR of 1.6 or more as determined by 18F-FDG uptake measured by PET scanning
* Patient must be on a stable dose for at least 8 weeks before baseline if taking medications used to control angina, hypertension, serum lipids (including statins) or any medication that can have an effect on inflammation
* Female patient is either not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practices a birth control method throughout the study and for 30 days after study completion
* Patient is judged to be in good general health as determined by the principal investigator
* Patient must be able and willing to comply with the requirements of this study protocol
Exclusion Criteria:
Poorly controlled medical condition, such as uncontrolled diabetes, documented history of recurrent infections, unstable ischemic heart disease, congestive heart failure, a left ventricular ejection fraction of less than 40%, recent stroke (within the past 3 months), chronic leg ulcer or any other condition which, in the opinion of the investigator, would put the patient at risk if participating in the study
* History of ACS, PCI, myocardial infarction, carotid revascularization or hospitalization for a cardiac condition within 12 weeks of baseline
* Prior coronary artery bypass graft
* Planned change in medical treatment during the study, that can have effect on inflammation, for angina, serum lipids, and other conditions
* History of cancer or lymphoproliferative disease other than a successfully treated non-metastatic cutaneous squamous cell or basal cell carcinoma and/or localized carcinoma in situ of the cervix
* History of listeriosis, treated or untreated tuberculosis, persistent chronic infections, or recent active infections requiring hospitalization or treatment with intravenous anti-infective agent within 30 days or oral anti-infective agent within 14 days prior to baseline
* Hepatitis B or hepatitis C viral infection
* Inflammatory bowel disease (Crohn's disease or ulcerative colitis) or patient with chronic diarrhea
* Pre-existent progressive neuromuscular disease or patient with creatine phosphokinase (CPK) level \> 3 times the upper limit of normal at baseline
* Current use or plans to use anti-retroviral therapy at any time during the study, or with active chronic disease often treated with a protease inhibitor, including AIDS
* Diagnosed with immune deficiency or as immunocompromised
* Any of the following: hemoglobin \< 120g/L, white blood cell count \< 3.0 X 109/L, platelet count \<130 X 109/L, Alanine aminotransferase (ALT) \> 3 times the upper limit of normal, Aspartate aminotransferase (AST) \> 3 times the upper normal limit, total bilirubin \> 2 times the upper normal limit, creatinine \> 150 umol/L, creatinine clearance \< 30 mL/min, or history of cirrhosis or severe hepatic disease
* Pregnant or breast-feeding or considering becoming pregnant during the study or for 6 months after the last dose of study medication
* History of clinically significant drug or alcohol abuse in the last year
* Previous bilateral carotid surgery
* Other indications for colchicine use (mainly chronic indications represented by Familial Mediterranean Fever or gout)
* History of an allergic reaction or significant sensitivity to constituents of study drug
* Use of an investigational chemical agent less than 50 days or 5 half-lives prior to baseline (whichever is longer)
* Judged by the investigator to be an unsuitable candidate for the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT02162303
Study Brief:
Protocol Section:
NCT02162303