Cohorte Française Des Patients Implantés de Micra AV

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 110
Healthy Volunteers: f
View:

• All patients who underwent Micra AV implantation

Locations
Other Locations
France
Paris Cardiovascular Research Centre (AV-CESAR Investigators)
RECRUITING
Paris
Contact Information
Primary
Eloi Marijon, MD,PhD
eloi.marijon@inserm.fr
+33662833848
Backup
Fawzi Kerkouri, MD
eecmcfawzikerkouri@gmail.com
+33767149558
Time Frame
Start Date: 2023-05-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 1000
Related Therapeutic Areas
Sponsors
Collaborators: Clinique Saint Augustin - Bordeaux, Centre Hospitalier Annecy Genevois, University Hospital, Montpellier, Clinique du Millenaire, Médipôle Lyon-Villeurbanne, University Hospital, Caen, Hospices Civils de Lyon, Central Hospital, Nancy, France, Hopital Prive Saint Martin - Bordeaux, Nantes University Hospital, Clinique Pasteur Toulouse, Centre Hospitalier Universitaire Dijon, Hospital Ambroise Paré Paris, Clinique Saint Pierre - Perpignan, Poitiers University Hospital, Institute Arnault Tzanck, France, University Hospital, Limoges, Institut Mutualiste Montsouris, Infirmerie Protestante Lyon, Centre Hospitalier Universitaire de Besancon, CHU de Reims, University Hospital, Angers, Institut Jacques Cartier - Massy, Clinique de la Sauvegarde - Lyon, University Hospital, Toulouse, CHU de Lille, University Hospital, Bordeaux, Centre Hospitalier Régional Metz-Thionville, European Georges Pompidou Hospital, Hôpital de la Timone, CHU de Rouen - Accueil, University Hospital, Strasbourg, France, Bichat Hospital, Hôpital Privé de Lille Métropole, Clinique Saint-Gatien - Tours, Rennes University Hospital, University Hospital, Clermont-Ferrand, CHU de Fort de France - Martinique, University Hospital of Saint-Etienne, Henri Mondor University Hospital, Centre Cardio-Thoracique de Monaco, Hospital St. Joseph, Marseille, France, Centre Hospitalier Régional et Universitaire de Brest, Hôpital privé Clairval - Marseille, CHU de Tours, Centre Hospitalier de Lens, Hôpital Privé de Parly II - Le Chesnay, University Hospital, Grenoble, Centre Hospitalier Universitaire, Amiens, Universite de La Reunion, Hôpital Privé Les Franciscaines
Leads: Paris Sudden Death Expertise Center

This content was sourced from clinicaltrials.gov