The Conus Brugada Syndrome Study (Conus-BRS)

Barts & The London NHS Trust

Status: Completed

Conditions: Brugada Syndrome

Study type: Observational

Funder types: Other

Identifiers

NCT06653504

Version 1 08/12/2016

Details and patient eligibility

About

An observational, analytical, cross sectional study investigating the effects of Conus branch and Right Ventricular (RV) Branch occlusion on surface ECG and intra-cardiac electrograms in patients undergoing percutaneous coronary intervention (PCI).

Enrollment: 3 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

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