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 @ 2:34 PM
Ignite Modification Date: 2025-12-24 @ 2:34 PM
NCT ID: NCT03227159
Eligibility Criteria: Inclusion Criteria: * Only patients who are able to give consent. This has to be carefully verified in each case, by the doctors leading the study * Men or women \>18 and \<85 years of age * Patients with chest discomfort within last 24h and suspected Acute Coronary Syndrome (STEMI, NSTEMI and unstable angina) * Patient experiencing at least 30 minutes of chest discomfort or other symptoms consistent with possible ACS; (Note: Patients who have symptoms of shorter duration that resolved due to pharmacologic intervention may be included.) * Written informed consent Exclusion Criteria: * Age \<18 or \>85 years * Inpatient in the hospital prior to onset of symptoms. * Obvious traumatic disease * Prisoners or other institutionalized or vulnerable individuals * Major surgery within last 4 weeks * Patients with cardiogenic shock * Other significant laboratory abnormalities that the investigator feels may compromise the patient's safety by participation in the study * Women who are pregnant or breast feeding * Obvious iv drug abuse * Refusal to provide written informed consent * Unavailability of a telephone number and insufficient contact information as well as permanent residence abroad * Unreliability as a study participant as based on the investigator's prior knowledge of the patient, such as the inability or willingness to participate in or complete the study or the presence of concurrent physical or psychological disorders that may make it impractical for the patient to participate in or complete the study
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT03227159
Study Brief:
Protocol Section: NCT03227159