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 @ 9:19 PM
Ignite Modification Date:
2025-12-24 @ 9:19 PM
NCT ID:
NCT03338504
Eligibility Criteria:
Inclusion Criteria:
* Unscheduled hospital admission with acute myocardial injury (defined as a rise and or fall in high-sensitivity cardiac troponin I concentrations on blood testing)
* A suspected aetiology of myocardial oxygen supply and demand imbalance with symptoms or signs of myocardial ischaemia
Exclusion Criteria:
* Unable or unwilling to give informed consent
* Women who are pregnant, breastfeeding or of child-bearing potential (women who have experienced menarche, are pre-menopausal and have not been sterilised) will not be enrolled into the trial.
* Probable type 1 myocardial infarction
* Renal impairment (estimated glomerular filtration rate ≤30ml/min/1.73m2)
* Severe hepatic impairment
* Frailty with inability to self-transfer (determined using Katz Index)
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT03338504
Study Brief:
Protocol Section:
NCT03338504