At a glance
ClinicalIndex Comparison RecordN/ACompleted· 206 enrolled
Drug / intervention
RF ablation, using specialized CFAE softwareprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
EXPRESSO - European Carto® XP REgistry for Validating Specialized CFAE SOftware
In Brief
An observational study evaluating RF ablation, using specialized CFAE software for Atrial Fibrillation. Completed, enrolled 206 participants across 13 sites in 3 countries.
Detailed Summary
The purpose of this prospective observational study (registry) is to determine the acute success rate of a complex fractionated atrial electrogram (CFAE) guided ablation procedure using a dedicated software and to determine the functionality and performance of the CFAE software in patients with a type of persistent atrial fibrillation (AF) in routine clinical practice.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsAtrial Fibrillation
CountriesFrance, Germany, Hungary
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartSep 2008
First PostedDec 2008
Primary CompletionSep 2010
Study CompletionDec 2010
TodayJul 2026
First PostedDec 22, 2008
Enrollment StartSep 1, 2008
Primary CompletionSep 1, 2010
Study CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 17.5 years ago
Interventions
RF ablation, using specialized CFAE softwareprocedure
RF ablation