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:
2025-12-25 @ 4:07 AM
Ignite Modification Date:
2025-12-25 @ 4:07 AM
NCT ID:
NCT07112820
Eligibility Criteria:
Inclusion Criteria:
* Patient over 18 years of age
* Hospitalised in cardiology as an emergency for acute coronary syndrome without ST segment elevation with indication for coronary angiography within 72 hours of admission
* Not yet undergone coronary angiography.
* Troponin \>99th percentile, i.e. \>27ng/l (troponin I, hypersensitive, Abbott)
* With de novo segmental kinetic disorder on TTE or ECG repolarisation disorder outside ST elevation
* Patient affiliated with a health insurance scheme
* French-speaking patient
* Patient who has given their free, informed and written consent
Exclusion Criteria:
Haemodynamically unstable patient: HR \> 100 and/or systolic blood pressure \< 90 mmHg and/or diastolic blood pressure \< 60 mmHg and/or oxygen saturation \< 92% in AA and/or clinical signs of hypoperfusion (mottling, cyanosis)
* Rhythmically unstable patient: sustained ventricular tachycardia, sudden death recovered.
* Patient with a known allergy to ultrasound contrast medium
* Patient with ST segment elevation.
* Patient with a contraindication to MRI.
* Patient with a caricatured picture of myocarditis (fever and/or significant biological inflammatory syndrome with CRP\>50mg/l)
* Patients already included in a type 1 interventional research protocol (RIPH1)
* Patients under guardianship or curatorship
* Patients deprived of their liberty
* Patients under judicial protection
* Pregnant or breastfeeding patients (negative pregnancy test for women of childbearing age)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07112820
Study Brief:
Protocol Section:
NCT07112820