Atrial Fibrillation Clinical Trial
Official title:
Oesophageal Probe Evaluation in RF Ablation of Atrial Fibrillation
The Trial will evaluate the influence of oesophageal probes in Radio frequency (RF)-ablation of atrial fibrillation regarding oesophageal ulcers after ablation.
The Trial will evaluate the influence of oesophageal probes in RF-ablation of atrial
fibrillation regarding oesophageal complications after ablation.
200 patients will be prospectively randomised into 2 groups. The conventional group will
undergo RF-Ablation of atrial fibrillation using an oesophageal probe to measure the
temperature during ablation.
In the other group will receive ablation using fixed energy levels (25 Watt) at the posterior
left atrial (LA) Wall without an oesophageal probe , All patients will get a gastroscopy for
evaluation of oesophageal complications the day after the procedure.
All patients will have a 6 months follow up (FU) in our clinic to be reevaluated for
complications (primary endpoint) and rhythm stability. (secondary endpoint)
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