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: 2025-12-26 @ 12:19 PM
Ignite Modification Date: 2025-12-26 @ 12:19 PM
NCT ID: NCT03438500
Eligibility Criteria: Inclusion Criteria: * History of anginal chest pain that prompted a myocardial stress test (nuclear myocardial perfusion imaging, stress echocardiography, or perfusion CMR) * Evidence for stress-induced myocardial ischemia in this examination * Coronary angiogram showing absence of ≥30% stenosis of epicardial coronary arteries Exclusion Criteria: * Participation in other clinical trials * age \<18 years * Contraindications to under cMRI * Contraindications to adenosine (severe chronic obstructive pulmonary disease (COPD), asthma, atrioventricular block (AV block) \> grade 1) * Left ventricular thrombus * Uncontrolled diabetes mellitus * Uncontrolled arterial hypertension, * Any other severe chronic illness such as liver or renal failure (glomerular filtration rate (GFR) \< 45 ml/min), active neoplastic disease, history of myocardial infarction or coronary revascularization within the past three months * Patients with pacemaker or implanted cardioverter defibrillator * Patients after valve surgical replacement * Patients after interventional valve replacement or reconstruction (e.g. transfemoral aortic valve replacement or MitraClip implantation) * Pregnancy (a reliable method of contraception must be used for the entire duration of the study) * Fertile female participants who are capable of bearing children and who do not use a method of contraception that is medically approved by the health authority of the respective country * Missing capacity to consent
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT03438500
Study Brief:
Protocol Section: NCT03438500