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 @ 11:42 PM
Ignite Modification Date:
2025-12-24 @ 11:42 PM
NCT ID:
NCT06146751
Eligibility Criteria:
Inclusion criteria:
1. Age ≥ 18 years and ≤ 80 years;
2. Patients with left ventricular aneurysm detected by transthoracic echocardiography or 180±30 days after percutaneous ventricular reconstruction;
3. An informed consent form was signed voluntarily by the patients or an authorised family member.
Exclusion criteria:
1. Patients unable to lie down for any reason;
2. Patients who are unable to undergo MRI for psychological (e.g. suffering from claustrophobia syndrome) or physical reasons (e.g. non-antimagnetic metal retention in the body, hearing impairment, involuntary body movements, etc.);
3. Patients with a known history of iron allergy or hypersensitivity;
4. Patients taking other oral or intravenous iron products;
5. Patients with haemosiderin deposition or haemochromatosis;
6. Pregnant or lactating women;
7. Any other patient that the investigator deems inappropriate for enrolment.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT06146751
Study Brief:
Protocol Section:
NCT06146751