CompletedNot Applicable

The Conus Brugada Syndrome Study

United Kingdom3 participantsStarted 2018-11-05

Plain-language summary

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).

Who can participate

Age range18 Years – 85 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

ECG and/or electrogram changes

Timeframe: During Procedure

Trial details

NCT IDNCT06653504

SponsorBarts & The London NHS Trust

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-11-06

View on ClinicalTrials.gov More Brugada Syndrome trials