Atrial Fibrillation Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are at least 18 years old at the time of giving consent
- People who are scheduled to have a catheter ablation procedure to treat atrial flutter or atrial fibrillation (irregular heart rhythms), as recommended by their doctor and in line with current medical guidelines
- People who are able to understand the study information and are willing to sign a consent form
- People who are able and willing to attend all required study visits at an approved study location
Who may not be able to join:
- People for whom the VERAFEYE Imaging Catheter cannot be safely or practically used, as determined by their doctor
- Women who are pregnant or who plan to become pregnant during the study (at the time of enrolment, women must either be documented as unable to become pregnant, or have had a negative pregnancy test within the 7 days before the procedure)
- People who have side effects or complications from a previous invasive procedure that have not yet healed or resolved
- People who have any other planned surgery or procedure involving blood vessels within 30 days before or after the ablation procedure
- People whose life expectancy is less than 12 months
- People who currently have a blood clot in the left atrium (upper left chamber of the heart) — a clot check is required within 48 hours before or during the procedure, and if a clot is found, the procedure will not go ahead until a follow-up check confirms the clot is gone (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 0894352047
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Acute procedural success rates during the index procedure
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.