← Eichor
Study identifier: NCT05165095 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Clinical Assessment of Essential Remote Monitoring Functions in Pacemakers

Condition: Bradycardia · Remote Monitoring  ·  Sponsor: MicroPort CRM

PhaseN/A
Planned participants206
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of the clinical investigation is to document the safety and the performances of the remote monitoring functions of the ALIZEA, BOREA and CELEA pacemakers, i.e. the RAAT, the RVAT and the remote alerts.

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

Talk to the study team

Antoine Guihard  ·  +33 1 46 01 33 20  ·  antoine.guihard@crm.microport.com

Always discuss trial participation with your own doctor first.

Locations (19)

Universitätsklinikum KremsKrems, AustriaRecruiting
Allgemeines Krankenhaus WienVienna, AustriaRecruiting
Clinique Saint JosephArlon, BelgiumRecruiting
CHU BordeauxBordeaux, FranceRecruiting
CH ChartresLe Coudray, FranceRecruiting
CHU Hôpital de la TimoneMarseille, FranceRecruiting
CHU NantesNantes, FranceRecruiting
Clinique Pasteur ToulouseToulouse, FranceRecruiting
CH ValenceValence, FranceRecruiting
Cardiologicum HamburgHamburg, GermanyRecruiting
Cardiologicum PirnaPirna, GermanyRecruiting
Kardiologische Praxis Dr. Trautwein & Dr. PlackeRostock, GermanyRecruiting

+ 7 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05165095