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 @ 11:07 PM
Ignite Modification Date:
2025-12-24 @ 11:07 PM
NCT ID:
NCT07295769
Eligibility Criteria:
Inclusion Criteria:
Participants may take part in this clinical study only if they meet all of the following criteria:
1. Adults aged 19 years or older who voluntarily provide written informed consent to participate in the study
2. Patients diagnosed with ESUS (Embolic Stroke of Undetermined Source)
3. Patients who require in-hospital or out-of-hospital electrocardiographic (ECG) monitoring
Exclusion Criteria:
Participants who meet any of the following criteria cannot be enrolled in this clinical study:
1. Individuals already diagnosed with atrial fibrillation or atrial flutter
2. Individuals with a clearly identified cause of stroke
3. Individuals known to have allergic reactions to adhesives or hydrogels
4. Individuals who, in the investigator's judgment, have cognitive vulnerability that makes it difficult to understand the study information and voluntarily decide on participation
5. Any other individuals whom the principal investigator considers to be at potential risk by participating in the study or otherwise unsuitable for participation
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT07295769
Study Brief:
Protocol Section:
NCT07295769