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 @ 10:14 PM
Ignite Modification Date:
2025-12-24 @ 10:14 PM
NCT ID:
NCT02614235
Eligibility Criteria:
Inclusion Criteria:
* Patients with syncope refered to perform 24-hours conventional Holter who fulfill at least one of the following conditions:
1. ≥2 episodes of syncope in the last year, provided that they are not typical vasovagal syncope, and/or
2. ≥1 episode of syncope with any criterion of suspicion of cardiac-arrhythmic aetiology, according to current European Guidelines about management of syncope
Exclusion Criteria:
* Carrier of any cardiac implantable electronic device or internal loop recorder, as well as stablished indication for it according to current guidelines.
* Aetiologic diagnosis of syncope already known.
* Left ventricular ejection fraction ≤35%.
* Unability to perform the monitorization
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02614235
Study Brief:
Protocol Section:
NCT02614235