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Study identifier: NCT05953558 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

French Cohort Evaluating the effectiveneSs of Atrioventricular Synchrony by the micRa AV

Condition: Atrioventricular Synchrony by the Micra AV  ·  Sponsor: Paris Sudden Death Expertise Center

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to 110 Years
Healthy volunteersNo

About this study

Transvenous cardiac pacemakers have pitfalls due to lead- and device pocket-related complications. Leadless pacemakers were developed and introduced into clinical practice to overcome the weaknesses of traditional transvenous pacemakers. The absence of atrial pacing has restricted their uses mainly for cases of paroxysmal atrioventricular block (AVB) or AVB with atrial fibrillation. The Micra AV contains an embedded accelerometer that senses the atrial contraction waveform, allowing the ventricle to be paced once the atrial contraction is complete. This atrioventricular synchronization is intended to extend the use of the device to cases of permanent complete AVB with normal sinus function. Two randomized clinicals trials have been proven it's efficacy. However, with AV-CESAR cohort, we aim to evaluate the real word effectiveness of Micra AV, in the first 1000 patients implanted by the device in France.

This description comes directly from the study's public registry record.

Talk to the study team

Eloi Marijon, MD,PhD  ·  +33662833848  ·  eloi.marijon@inserm.fr

Fawzi Kerkouri, MD  ·  +33767149558  ·  eecmcfawzikerkouri@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Paris Cardiovascular Research Centre (AV-CESAR Investigators)Paris, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05953558