Eligibility Module

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 @ 4:35 PM
Ignite Modification Date: 2025-12-24 @ 4:35 PM
NCT ID: NCT02211066
Eligibility Criteria: Inclusion Criteria: * Patients of both sexes, older than 18 years old. * Written informed consent obtained. * Patients with stable angina pectoris (Canadian Cardiovascular Society (CCS) Class 1, 2, 3 or 4) or patients with documented silent ischemia by stress test during the last year. * Patients eligible for coronary revascularization in a coronary chronic total occlusion, which was angiographically documented in a previous coronary angiography during the last year. Exclusion Criteria: * Women who are pregnant or women of childbearing potential who do not use adequate contraception. * Known allergies to aspirin, clopidogrel bisulfate (Plavix ®), ticagrelor (BriliqueTM) heparin, or a sensitivity to contrast media, which cannot be adequately pre-medicated. * Participation in other studies. * Life expectancy of less than one year or factors making clinical and/or angiographic follow-up difficult. * Planned cardiac surgery or major non-cardiac surgery. * The subject has a history of bleeding diathesis or coagulopathy. * The subject suffered disabling stroke within the past year. * Known major hematologic, neoplastic, metabolic, gastrointestinal or endocrine dysfunction, which, in the judgment of the Investigator, may affect the patient's ability to complete the study. * History of malignancy, except in patients who have been disease-free \>5 years or whose only malignancy has been basal or squamous cell skin carcinoma. * Inability to provide informed consent
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02211066
Study Brief:
Protocol Section: NCT02211066