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 @ 7:55 PM
Ignite Modification Date:
2025-12-24 @ 7:55 PM
NCT ID:
NCT06653504
Eligibility Criteria:
Inclusion Criteria:
* Aged 18-85
* Patients able and willing to give their written informed consent.
* Planned PCI of a CTO of a right coronary artery
* Planned use of an anchor balloon in the Conus branch or RV branch
Exclusion Criteria:
* Patients considered unsuitable to participate by the research team (e.g., due to medical reasons, laboratory abnormalities, or subject's unwillingness to comply with all study related procedures).
* Patients with a pre-existing, confirmed or possible diagnosis of Brugada Syndrome
* Marked ST elevation or J point elevation on baseline (prior to procedure) ECG in the precordial leads (V1-V3)
* Pregnancy. This will be tested by urine HcG measurement
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT06653504
Study Brief:
Protocol Section:
NCT06653504